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| Product NDC Code | 43353-964 | ||||
|---|---|---|---|---|---|
| Drug Name | Pravastatin sodium |
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| Type | Generic | ||||
| Pharm Class | HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA] |
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| Active Ingredients |
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| Route | ORAL | ||||
| Dosage Form | TABLET | ||||
| RxCUI drug identifier | 904475, 904481 |
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| Application Number | ANDA076056 | ||||
| Labeler Name | Aphena Pharma Solutions - Tennessee, LLC | ||||
| Packages |
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| Check if available Online | Get Medication Prices online with Discount |
Overdosage of Pravastatin Sodium
Information about signs, symptoms, and laboratory findings of acute ovedosage and the general principles of overdose treatment.10 OVERDOSAGE To date, there has been limited experience with overdosage of pravastatin. If an overdose occurs, it should be treated symptomatically with laboratory monitoring and supportive measures should be instituted as required.
Adverse reactions
Information about undesirable effects, reasonably associated with use of the drug, that may occur as part of the pharmacological action of the drug or may be unpredictable in its occurrence. Adverse reactions include those that occur with the drug, and if applicable, with drugs in the same pharmacologically active and chemically related class. There is considerable variation in the listing of adverse reactions. They may be categorized by organ system, by severity of reaction, by frequency, by toxicological mechanism, or by a combination of these.6 ADVERSE REACTIONS Pravastatin is generally well tolerated; adverse reactions have usually been mild and transient. In 4 month-long placebo-controlled trials, 1.7% of pravastatin-treated patients and 1.2% of placebo-treated patients were discontinued from treatment because of adverse experiences attributed to study drug therapy; this difference was not statistically significant. In short-term clinical trials, the most commonly reported adverse reactions (≥ 2% and > placebo) regardless of causality were: musculoskeletal pain, nausea/vomiting, upper respiratory infection, diarrhea, and headache. ( 6.1 ) To report SUSPECTED ADVERSE REACTIONS, contact AvKARE, Inc. 1-8 55-361-3993 o r [email protected] ; or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch. 6.1 Adverse Clinical Events Short-Term Controlled Trials In the pravastatin sodium placebo-controlled clinical trials database of 1313 patients (age range 20 to 76 years, 32.4% women, 93.5% Caucasians, 5% Blacks, 0.9% Hispanics, 0.4% Asians, 0.2% Others) with a median treatment duration of 14 weeks, 3.3% of patients on pravastatin sodium and 1.2% patients on placebo discontinued due to adverse events regardless of causality. The most common adverse reactions that led to treatment discontinuation and occurred at an incidence greater than placebo were: liver function test increased, nausea, anxiety/depression, and dizziness. All adverse clinical events (regardless of causality) reported in ≥ 2% of pravastatin-treated patients in placebo-controlled trials of up to 8 months duration are identified in Table 1 : Table 1: Adverse Events in ≥ 2% of Patients Treated With Pravastatin 5 to 40 mg and at an Incidence Greater Than Placebo in Short-Term Placebo-Controlled Trials (% of Patients) 5 mg 10 mg 20 mg 40 mg Any Dose Placebo Body System/Event N = 100 N = 153 N = 478 N = 171 N = 902 N = 411 Cardiovascular Angina Pectoris 5 4.6 4.8 3.5 4.5 3.4 Dermatologic Rash 3 2.6 6.7 1.2 4.5 1.4 Gastrointestinal Nausea/Vomiting 4 5.9 10.5 2.3 7.4 7.1 Diarrhea 8 8.5 6.5 4.7 6.7 5.6 Flatulence 2 3.3 4.6 0 3.2 4.4 Dyspepsia/Heartburn 0 3.3 3.6 0.6 2.5 2.7 Abdominal Distension 2 3.3 2.1 0.6 2 2.4 General Fatigue 4 1.3 5.2 0 3.4 3.9 Chest Pain 4 1.3 3.3 1.2 2.7 1.9 Influenza 4 2.6 1.9 0.6 2 0.7 Musculoskeletal Musculoskeletal Pain 13 3.9 13.2 5.3 10.1 10.2 Myalgia 1 2.6 2.9 1.2 2.3 1.2 Nervous System Headache 5 6.5 7.5 3.5 6.3 4.6 Dizziness 4 1.3 5.2 0.6 3.5 3.4 Respiratory Pharyngitis 2 4.6 1.5 1.2 2 2.7 Upper Respiratory Infection 6 9.8 5.2 4.1 5.9 5.8 Rhinitis 7 5.2 3.8 1.2 3.9 4.9 Cough 4 1.3 3.1 1.2 2.5 1.7 Investigation ALT Increased 2 2 4 1.2 2.9 1.2 g-GT Increased 3 2.6 2.1 0.6 2 1.2 CPK Increased 5 1.3 5.2 2.9 4.1 3.6 The safety and tolerability of pravastatin sodium at a dose of 80 mg in 2 controlled trials with a mean exposure of 8.6 months was similar to that of pravastatin sodium at lower doses except that 4 out of 464 patients taking 80 mg of pravastatin had a single elevation of CK > 10 times ULN compared to 0 out of 115 patients taking 40 mg of pravastatin. Long-Term Controlled Morbidity and Mortality Trials In the pravastatin sodium placebo-controlled clinical trials database of 21,483 patients (age range 24 to 75 years, 10.3% women, 52.3% Caucasians, 0.8% Blacks, 0.5% Hispanics, 0.1% Asians, 0.1% Others, 46.1% Not Recorded) with a median treatment duration of 261 weeks, 8.1% of patients on pravastatin sodium and 9.3% patients on placebo discontinued due to adverse events regardless of causality. Adverse event data were pooled from several double-blind, placebo-controlled trials (e.g., West of Scotland Coronary Prevention Study [WOS]; Pravastatin Limitation of Atherosclerosis in the Coronary Arteries study [PLAC I]; Pravastatin, Lipids and Atherosclerosis in the Carotids study [PLAC II]; Regression Growth Evaluation Statin Study [REGRESS]; and Kuopio Atherosclerosis Prevention Study [KAPS]) involving a total of 10,764 patients treated with pravastatin 40 mg and 10,719 patients treated with placebo. The safety and tolerability profile in the pravastatin group was comparable to that of the placebo group. Patients were exposed to pravastatin for a mean of 4 to 5.1 years in, among other trials, WOS and 1.9 to 2.9 years in PLAC I, PLAC II, KAPS, and REGRESS. In these long-term trials, the most common reasons for discontinuation were mild, non-specific gastrointestinal complaints. Collectively, these trials represent 47,613 patient-years of exposure to pravastatin. All clinical adverse events (regardless of causality) occurring in ≥ 2% of patients treated with pravastatin in these studies are identified in Table 2 . Table 2: Adverse Events in ≥ 2% of Patients Treated With Pravastatin 40 mg and at an Incidence Greater Than Placebo in Long-Term Placebo-Controlled Trials Pravastatin Placebo (N = 10,764) (N = 10,719) Body System/Event % of patients % of patients Dermatologic Rash (including dermatitis) 7.2 7.1 General Edema 3 2.7 Fatigue 8.4 7.8 Chest Pain 10 9.8 Fever 2.1 1.9 Weight Gain 3.8 3.3 Weight Loss 3.3 2.8 Musculoskeletal Musculoskeletal Pain 24.9 24.4 Muscle Cramp 5.1 4.6 Musculoskeletal Traumatism 10.2 9.6 Nervous System Dizziness 7.3 6.6 Sleep Disturbance 3 2.4 Anxiety/Nervousness 4.8 4.7 Paresthesia 3.2 3 Renal/Genitourinary Urinary Tract Infection 2.7 2.6 Respiratory Upper Respiratory Tract Infection 21.2 20.2 Cough 8.2 7.4 Influenza 9.2 9 Pulmonary Infection 3.8 3.5 Sinus Abnormality 7 6.7 Tracheobronchitis 3.4 3.1 Special Senses Vision Disturbance (includes blurred vision, diplopia) 3.4 3.3 Infections Viral Infection 3.2 2.9 In addition to the events listed above in the long-term trials table, events of probable, possible, or uncertain relationship to study drug that occurred in < 2% of pravastatin-treated patients in the long-term trials included the following: Dermatologic: scalp hair abnormality (including alopecia), urticaria. Endocrine/Metabolic: sexual dysfunction, libido change. General: flushing. Immunologic: allergy, edema head/neck. Musculoskeletal: muscle weakness. Nervous System: vertigo, insomnia, memory impairment, neuropathy (including peripheral neuropathy). Special Senses: taste disturbance. 6.2 Postmarketing Experience In addition to the events reported above, as with other drugs in this class, the following events have been reported rarely during postmarketing experience with pravastatin sodium, regardless of causality assessment: Musculoskeletal: myopathy, rhabdomyolysis. There have been rare reports of immune-mediated necrotizing myopathy associated with statin use [see Warnings and Precautions ( 5.1 ) ]. Nervous System: dysfunction of certain cranial nerves (including alteration of taste, impairment of extraocular movement, facial paresis), peripheral nerve palsy. There have been rare postmarketing reports of cognitive impairment (e.g., memory loss, forgetfulness, amnesia, memory impairment, confusion) associated with statin use. These cognitive issues have been reported for all statins. The reports are generally nonserious, and reversible upon statin discontinuation, with variable times to symptom onset (1 day to years) and symptom resolution (median of 3 weeks). Hypersensitivity: anaphylaxis, angioedema, lupus erythematosus-like syndrome, polymyalgia rheumatica, dermatomyositis, vasculitis, purpura, hemolytic anemia, positive ANA, ESR increase, arthritis, arthralgia, asthenia, photosensitivity, chills, malaise, toxic epidermal necrolysis, erythema multiforme (including Stevens-Johnson syndrome). Gastrointestinal: abdominal pain, constipation, pancreatitis, hepatitis (including chronic active hepatitis), cholestatic jaundice, fatty change in liver, cirrhosis, fulminant hepatic necrosis, hepatoma, fatal and non-fatal hepatic failure. Dermatologic: a variety of skin changes (e.g., nodules, discoloration, dryness of mucous membranes, changes to hair/nails). Renal: urinary abnormality (including dysuria, frequency, nocturia). Respiratory: dyspnea. Reproductive: gynecomastia. Laboratory Abnormalities: liver function test abnormalities, thyroid function abnormalities. 6.3 Laboratory Test Abnormalities Increases in ALT, AST values and CPK have been observed [ see Warnings and Precautions ( 5.1 , 5.2 ) ]. Transient, asymptomatic eosinophilia has been reported. Eosinophil counts usually returned to normal despite continued therapy. Anemia, thrombocytopenia, and leukopenia have been reported with statins. 6.4 Pediatric Patients In a 2 year, double-blind, placebo-controlled study involving 100 boys and 114 girls with HeFH (n = 214; age range 8 to 18.5 years, 53% female, 95% Caucasians, < 1% Blacks, 3% Asians, 1% Other), the safety and tolerability profile of pravastatin was generally similar to that of placebo [ see Warnings and Precautions ( 5.3 ), Use in Specific Populations ( 8.4 ), and Clinical Pharmacology ( 12.3 ) ].
| Cardiovascular | ||||||
| Angina Pectoris | 5 | 4.6 | 4.8 | 3.5 | 4.5 | 3.4 |
| Dermatologic | ||||||
| Rash | 3 | 2.6 | 6.7 | 1.2 | 4.5 | 1.4 |
| Gastrointestinal | ||||||
| Nausea/Vomiting | 4 | 5.9 | 10.5 | 2.3 | 7.4 | 7.1 |
| Diarrhea | 8 | 8.5 | 6.5 | 4.7 | 6.7 | 5.6 |
| Flatulence | 2 | 3.3 | 4.6 | 0 | 3.2 | 4.4 |
| Dyspepsia/Heartburn | 0 | 3.3 | 3.6 | 0.6 | 2.5 | 2.7 |
| Abdominal Distension | 2 | 3.3 | 2.1 | 0.6 | 2 | 2.4 |
| General | ||||||
| Fatigue | 4 | 1.3 | 5.2 | 0 | 3.4 | 3.9 |
| Chest Pain | 4 | 1.3 | 3.3 | 1.2 | 2.7 | 1.9 |
| Influenza | 4 | 2.6 | 1.9 | 0.6 | 2 | 0.7 |
| Musculoskeletal | ||||||
| Musculoskeletal Pain | 13 | 3.9 | 13.2 | 5.3 | 10.1 | 10.2 |
| Myalgia | 1 | 2.6 | 2.9 | 1.2 | 2.3 | 1.2 |
| Nervous System | ||||||
| Headache | 5 | 6.5 | 7.5 | 3.5 | 6.3 | 4.6 |
| Dizziness | 4 | 1.3 | 5.2 | 0.6 | 3.5 | 3.4 |
| Respiratory | ||||||
| Pharyngitis | 2 | 4.6 | 1.5 | 1.2 | 2 | 2.7 |
| Upper Respiratory Infection | 6 | 9.8 | 5.2 | 4.1 | 5.9 | 5.8 |
| Rhinitis | 7 | 5.2 | 3.8 | 1.2 | 3.9 | 4.9 |
| Cough | 4 | 1.3 | 3.1 | 1.2 | 2.5 | 1.7 |
| Investigation | ||||||
| ALT Increased | 2 | 2 | 4 | 1.2 | 2.9 | 1.2 |
| g-GT Increased | 3 | 2.6 | 2.1 | 0.6 | 2 | 1.2 |
| CPK Increased | 5 | 1.3 | 5.2 | 2.9 | 4.1 | 3.6 |
| Dermatologic | ||
| Rash (including dermatitis) | 7.2 | 7.1 |
| General | ||
| Edema | 3 | 2.7 |
| Fatigue | 8.4 | 7.8 |
| Chest Pain | 10 | 9.8 |
| Fever | 2.1 | 1.9 |
| Weight Gain | 3.8 | 3.3 |
| Weight Loss | 3.3 | 2.8 |
| Musculoskeletal | ||
| Musculoskeletal Pain | 24.9 | 24.4 |
| Muscle Cramp | 5.1 | 4.6 |
| Musculoskeletal Traumatism | 10.2 | 9.6 |
| Nervous System | ||
| Dizziness | 7.3 | 6.6 |
| Sleep Disturbance | 3 | 2.4 |
| Anxiety/Nervousness | 4.8 | 4.7 |
| Paresthesia | 3.2 | 3 |
| Renal/Genitourinary | ||
| Urinary Tract Infection | 2.7 | 2.6 |
| Respiratory | ||
| Upper Respiratory Tract Infection | 21.2 | 20.2 |
| Cough | 8.2 | 7.4 |
| Influenza | 9.2 | 9 |
| Pulmonary Infection | 3.8 | 3.5 |
| Sinus Abnormality | 7 | 6.7 |
| Tracheobronchitis | 3.4 | 3.1 |
| Special Senses | ||
| Vision Disturbance (includes blurred vision, diplopia) | 3.4 | 3.3 |
| Infections | ||
| Viral Infection | 3.2 | 2.9 |
Pravastatin Sodium Drug Interactions
Information about and practical guidance on preventing clinically significant drug/drug and drug/food interactions that may occur in people taking the drug.7 DRUG INTERACTIONS For the concurrent therapy of either cyclosporine, fibrates, niacin (nicotinic acid), or erythromycin, the risk of myopathy increases [ see Warnings and Precautions ( 5.1 ) and Clinical Pharmacology ( 12.3 ) ]. Concomitant lipid-lowering therapies: use with fibrates or lipid-modifying doses (≥ 1 g/day) of niacin increases the risk of adverse skeletal muscle effects. Caution should be used when prescribing with pravastatin sodium. ( 7 ) Cyclosporine: combination increases exposure. Limit pravastatin to 20 mg once daily. ( 2.5 , 7.1 ) Clarithromycin: combination increases exposure. Limit pravastatin to 40 mg once daily. ( 2.6 , 7.2 ) 7.1 Cyclosporine The risk of myopathy/rhabdomyolysis is increased with concomitant administration of cyclosporine. Limit pravastatin to 20 mg once daily for concomitant use with cyclosporine [ see Dosage and Administration ( 2.5 ), Warnings and Precautions ( 5.1 ), and Clinical Pharmacology ( 12.3 ) ]. 7.2 Clarithromycin The risk of myopathy/rhabdomyolysis is increased with concomitant administration of clarithromycin. Limit pravastatin to 40 mg once daily for concomitant use with clarithromycin [ see Dosage and Administration ( 2.6 ), Warnings and Precautions ( 5.1 ), and Clinical Pharmacology ( 12.3 ) ]. 7.3 Colchicine The risk of myopathy/rhabdomyolysis is increased with concomitant administration of colchicine [ see Warnings and Precautions ( 5.1 ) ]. 7.4 Gemfibrozil Due to an increased risk of myopathy/rhabdomyolysis when HMG-CoA reductase inhibitors are coadministered with gemfibrozil, concomitant administration of pravastatin sodium with gemfibrozil should be avoided [ see Warnings and Precautions ( 5.1 ) ]. 7.5 Other Fibrates Because it is known that the risk of myopathy during treatment with HMG-CoA reductase inhibitors is increased with concurrent administration of other fibrates, pravastatin sodium should be administered with caution when used concomitantly with other fibrates [ see Warnings and Precautions ( 5.1 ) ]. 7.6 Niacin The risk of skeletal muscle effects may be enhanced when pravastatin is used in combination with niacin; a reduction in pravastatin sodium dosage should be considered in this setting [ see Warnings and Precautions ( 5.1 ) ].
Clinical pharmacology
Information about the clinical pharmacology and actions of the drug in humans.12 CLINICAL PHARMACOLOGY 12.1 Mechanism of Action Pravastatin is a reversible inhibitor of 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase, the enzyme that catalyzes the conversion of HMG-CoA to mevalonate, an early and rate limiting step in the biosynthetic pathway for cholesterol. In addition, pravastatin reduces VLDL and TG and increases HDL-C. 12.3 Pharmacokinetics General Absorption: Pravastatin sodium is administered orally in the active form. In studies in man, peak plasma pravastatin concentrations occurred 1 to 1.5 hours upon oral administration. Based on urinary recovery of total radiolabeled drug, the average oral absorption of pravastatin is 34% and absolute bioavailability is 17%. While the presence of food in the gastrointestinal tract reduces systemic bioavailability, the lipid-lowering effects of the drug are similar whether taken with or 1 hour prior to meals. Pravastatin plasma concentrations, including area under the concentration-time curve (AUC), C max , and steady-state minimum (C min ), are directly proportional to administered dose. Systemic bioavailability of pravastatin administered following a bedtime dose was decreased 60% compared to that following an AM dose. Despite this decrease in systemic bioavailability, the efficacy of pravastatin administered once daily in the evening, although not statistically significant, was marginally more effective than that after a morning dose. The coefficient of variation (CV), based on between-subject variability, was 50% to 60% for AUC. The geometric means of pravastatin C max and AUC following a 20 mg dose in the fasted state were 26.5 ng/mL and 59.8 ng*hr/mL, respectively. Steady-state AUCs, C max , and C min plasma concentrations showed no evidence of pravastatin accumulation following once or twice daily administration of pravastatin sodium tablets. Distribution: Approximately 50% of the circulating drug is bound to plasma proteins. Metabolism: The major biotransformation pathways for pravastatin are: (a) isomerization to 6-epi pravastatin and the 3α-hydroxyisomer of pravastatin (SQ 31,906) and (b) enzymatic ring hydroxylation to SQ 31,945. The 3α-hydroxyisomeric metabolite (SQ 31,906) has 1/10 to 1/40 the HMG-CoA reductase inhibitory activity of the parent compound. Pravastatin undergoes extensive first-pass extraction in the liver (extraction ratio 0.66). Excretion: Approximately 20% of a radiolabeled oral dose is excreted in urine and 70% in the feces. After intravenous administration of radiolabeled pravastatin to normal volunteers, approximately 47% of total body clearance was via renal excretion and 53% by non-renal routes (i.e., biliary excretion and biotransformation). Following single dose oral administration of 14 C-pravastatin, the radioactive elimination t ½ for pravastatin is 1.8 hours in humans. Specific Populations Renal Impairment: A single 20 mg oral dose of pravastatin was administered to 24 patients with varying degrees of renal impairment (as determined by creatinine clearance). No effect was observed on the pharmacokinetics of pravastatin or its 3α-hydroxy isomeric metabolite (SQ 31,906). Compared to healthy subjects with normal renal function, patients with severe renal impairment had 69% and 37% higher mean AUC and C max values, respectively, and a 0.61 hour shorter t½ for the inactive enzymatic ring hydroxylation metabolite (SQ 31,945). Hepatic Impairment: In a study comparing the kinetics of pravastatin in patients with biopsy confirmed cirrhosis (N = 7) and normal subjects (N = 7), the mean AUC varied 18 fold in cirrhotic patients and 5 fold in healthy subjects. Similarly, the peak pravastatin values varied 47 fold for cirrhotic patients compared to 6 fold for healthy subjects [ see Warnings and Precautions ( 5.2 ) ]. Geriatric: In a single oral dose study using pravastatin 20 mg, the mean AUC for pravastatin was approximately 27% greater and the mean cumulative urinary excretion (CUE) approximately 19% lower in elderly men (65 to 75 years old) compared with younger men (19 to 31 years old). In a similar study conducted in women, the mean AUC for pravastatin was approximately 46% higher and the mean CUE approximately 18% lower in elderly women (65 to 78 years old) compared with younger women (18 to 38 years old). In both studies, C max , T max , and t ½ values were similar in older and younger subjects [ see Use in Specific Populations ( 8.5 ) ]. Pediatric: After 2 weeks of once-daily 20 mg oral pravastatin administration, the geometric means of AUC were 80.7 (CV 44%) and 44.8 (CV 89%) ng*hr/mL for children (8 to 11 years, N = 14) and adolescents (12 to 16 years, N = 10), respectively. The corresponding values for C max were 42.4 (CV 54%) and 18.6 ng/mL (CV 100%) for children and adolescents, respectively. No conclusion can be made based on these findings due to the small number of samples and large variability [ see Use in Specific Populations ( 8.4 ) ]. Drug-Drug Interactions Table 3: Effect of Coadministered Drugs on the Pharmacokinetics of Pravastatin Coadministered Drug and Dosing Regimen Pravastatin Dose (mg) Change in AUC Change in C max Cyclosporine 5 mg/kg single dose 40 mg single dose ↑282% ↑327% Clarithromycin 500 mg BID for 9 days 40 mg OD for 8 days ↑110% ↑128% Boceprevir 800 mg TID for 6 days 40 mg single dose ↑63% ↑49% Darunavir 600 mg BID/Ritonavir 100 mg BID for 7 days 40 mg single dose ↑81% ↑63% Colestipol 10 g single dose 20 mg single dose ↓47% ↓53% Cholestyramine 4 g single dose 20 mg single dose Administered simultaneously ↓40% ↓39% Administered 1 hour prior to cholestyramine ↑12% ↑30% Administered 4 hours after cholestyramine ↓12% ↓6.8% Cholestyramine 24 g OD for 4 weeks 20 mg BID for 8 weeks ↓51% ↑4.9% 5 mg BID for 8 weeks ↓38% ↑23% 10 mg BID for 8 weeks ↓18% ↓33% Fluconazole 200 mg IV for 6 days 20 mg PO + 10 mg IV ↓34% ↓33% 200 mg PO for 6 days 20 mg PO + 10 mg IV ↓16% ↓16% Kaletra 400 mg/100 mg BID for 14 days 20 mg OD for 4 days ↑33% ↑26% Verapamil IR 120 mg for 1 day and Verapamil ER 480 mg for 3 days 40 mg single dose ↑31% ↑42% Cimetidine 300 mg QID for 3 days 20 mg single dose ↑30% ↑9.8% Antacids 15 mL QID for 3 days 20 mg single dose ↓28% ↓24% Digoxin 0.2 mg OD for 9 days 20 mg OD for 9 days ↑23% ↑26% Probucol 500 mg single dose 20 mg single dose ↑14% ↑24% Warfarin 5 mg OD for 6 days 20 mg BID for 6 days ↓13% ↓6.7% Itraconazole 200 mg OD for 30 days 40 mg OD for 30 days ↑11% (compared to Day 1) ↑17% (compared to Day 1) Gemfibrozil 600 mg single dose 20 mg single dose ↓7% ↓20% Aspirin 324 mg single dose 20 mg single dose ↑4.7% ↑8.9% Niacin 1 g single dose 20 mg single dose ↓3.6% ↓8.2% Diltiazem 20 mg single dose ↑2.7% ↑30% Grapefruit juice 40 mg single dose ↓1.8% ↑3.7% BID = twice daily; OD = once daily; QID = four times daily Table 4: Effect of Pravastatin on the Pharmacokinetics of Coadministered Drugs Pravastatin Dosing Regimen Name and Dose Change in AUC Change in C max 20 mg BID for 6 days Warfarin 5 mg OD for 6 days ↑17% ↑15% Change in mean prothrombin time ↑0.4 sec 20 mg OD for 9 days Digoxin 0.2 mg OD for 9 days ↑4.6% ↑5.3% 20 mg BID for 4 weeks Antipyrine 1.2 g single dose ↑3% Not Reported 10 mg BID for 4 weeks ↑1.6% 5 mg BID for 4 weeks ↑ Less than 1% 20 mg OD for 4 days Kaletra 400 mg/100 mg BID for 14 days No change No change BID = twice daily; OD = once daily
| Cyclosporine 5 mg/kg single dose | 40 mg single dose | ↑282% | ↑327% |
| Clarithromycin 500 mg BID for 9 days | 40 mg OD for 8 days | ↑110% | ↑128% |
| Boceprevir 800 mg TID for 6 days | 40 mg single dose | ↑63% | ↑49% |
| Darunavir 600 mg BID/Ritonavir 100 mg BID for 7 days | 40 mg single dose | ↑81% | ↑63% |
| Colestipol 10 g single dose | 20 mg single dose | ↓47% | ↓53% |
| Cholestyramine 4 g single dose | 20 mg single dose | ||
| Administered simultaneously | ↓40% | ↓39% | |
| Administered 1 hour prior to cholestyramine | ↑12% | ↑30% | |
| Administered 4 hours after cholestyramine | ↓12% | ↓6.8% | |
| Cholestyramine 24 g OD for 4 weeks | 20 mg BID for 8 weeks | ↓51% | ↑4.9% |
| 5 mg BID for 8 weeks | ↓38% | ↑23% | |
| 10 mg BID for 8 weeks | ↓18% | ↓33% | |
| Fluconazole | |||
| 200 mg IV for 6 days | 20 mg PO + 10 mg IV | ↓34% | ↓33% |
| 200 mg PO for 6 days | 20 mg PO + 10 mg IV | ↓16% | ↓16% |
| Kaletra 400 mg/100 mg BID for 14 days | 20 mg OD for 4 days | ↑33% | ↑26% |
| Verapamil IR 120 mg for 1 day and Verapamil ER 480 mg for 3 days | 40 mg single dose | ↑31% | ↑42% |
| Cimetidine 300 mg QID for 3 days | 20 mg single dose | ↑30% | ↑9.8% |
| Antacids 15 mL QID for 3 days | 20 mg single dose | ↓28% | ↓24% |
| Digoxin 0.2 mg OD for 9 days | 20 mg OD for 9 days | ↑23% | ↑26% |
| Probucol 500 mg single dose | 20 mg single dose | ↑14% | ↑24% |
| Warfarin 5 mg OD for 6 days | 20 mg BID for 6 days | ↓13% | ↓6.7% |
| Itraconazole 200 mg OD for 30 days | 40 mg OD for 30 days | ↑11% (compared to Day 1) | ↑17% (compared to Day 1) |
| Gemfibrozil 600 mg single dose | 20 mg single dose | ↓7% | ↓20% |
| Aspirin 324 mg single dose | 20 mg single dose | ↑4.7% | ↑8.9% |
| Niacin 1 g single dose | 20 mg single dose | ↓3.6% | ↓8.2% |
| Diltiazem | 20 mg single dose | ↑2.7% | ↑30% |
| Grapefruit juice | 40 mg single dose | ↓1.8% | ↑3.7% |
| 20 mg BID for 6 days | Warfarin 5 mg OD for 6 days | ↑17% | ↑15% |
| Change in mean prothrombin time | ↑0.4 sec | ||
| 20 mg OD for 9 days | Digoxin 0.2 mg OD for 9 days | ↑4.6% | ↑5.3% |
| 20 mg BID for 4 weeks | Antipyrine 1.2 g single dose | ↑3% | Not Reported |
| 10 mg BID for 4 weeks | ↑1.6% | ||
| 5 mg BID for 4 weeks | ↑ Less than 1% | ||
| 20 mg OD for 4 days | Kaletra 400 mg/100 mg BID for 14 days | No change | No change |
Mechanism of action
Information about the established mechanism(s) of the drugÕs action in humans at various levels (for example receptor, membrane, tissue, organ, whole body). If the mechanism of action is not known, this field contains a statement about the lack of information.12.1 Mechanism of Action Pravastatin is a reversible inhibitor of 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase, the enzyme that catalyzes the conversion of HMG-CoA to mevalonate, an early and rate limiting step in the biosynthetic pathway for cholesterol. In addition, pravastatin reduces VLDL and TG and increases HDL-C.
Pharmacokinetics
Information about the clinically significant pharmacokinetics of a drug or active metabolites, for instance pertinent absorption, distribution, metabolism, and excretion parameters.12.3 Pharmacokinetics General Absorption: Pravastatin sodium is administered orally in the active form. In studies in man, peak plasma pravastatin concentrations occurred 1 to 1.5 hours upon oral administration. Based on urinary recovery of total radiolabeled drug, the average oral absorption of pravastatin is 34% and absolute bioavailability is 17%. While the presence of food in the gastrointestinal tract reduces systemic bioavailability, the lipid-lowering effects of the drug are similar whether taken with or 1 hour prior to meals. Pravastatin plasma concentrations, including area under the concentration-time curve (AUC), C max , and steady-state minimum (C min ), are directly proportional to administered dose. Systemic bioavailability of pravastatin administered following a bedtime dose was decreased 60% compared to that following an AM dose. Despite this decrease in systemic bioavailability, the efficacy of pravastatin administered once daily in the evening, although not statistically significant, was marginally more effective than that after a morning dose. The coefficient of variation (CV), based on between-subject variability, was 50% to 60% for AUC. The geometric means of pravastatin C max and AUC following a 20 mg dose in the fasted state were 26.5 ng/mL and 59.8 ng*hr/mL, respectively. Steady-state AUCs, C max , and C min plasma concentrations showed no evidence of pravastatin accumulation following once or twice daily administration of pravastatin sodium tablets. Distribution: Approximately 50% of the circulating drug is bound to plasma proteins. Metabolism: The major biotransformation pathways for pravastatin are: (a) isomerization to 6-epi pravastatin and the 3α-hydroxyisomer of pravastatin (SQ 31,906) and (b) enzymatic ring hydroxylation to SQ 31,945. The 3α-hydroxyisomeric metabolite (SQ 31,906) has 1/10 to 1/40 the HMG-CoA reductase inhibitory activity of the parent compound. Pravastatin undergoes extensive first-pass extraction in the liver (extraction ratio 0.66). Excretion: Approximately 20% of a radiolabeled oral dose is excreted in urine and 70% in the feces. After intravenous administration of radiolabeled pravastatin to normal volunteers, approximately 47% of total body clearance was via renal excretion and 53% by non-renal routes (i.e., biliary excretion and biotransformation). Following single dose oral administration of 14 C-pravastatin, the radioactive elimination t ½ for pravastatin is 1.8 hours in humans. Specific Populations Renal Impairment: A single 20 mg oral dose of pravastatin was administered to 24 patients with varying degrees of renal impairment (as determined by creatinine clearance). No effect was observed on the pharmacokinetics of pravastatin or its 3α-hydroxy isomeric metabolite (SQ 31,906). Compared to healthy subjects with normal renal function, patients with severe renal impairment had 69% and 37% higher mean AUC and C max values, respectively, and a 0.61 hour shorter t½ for the inactive enzymatic ring hydroxylation metabolite (SQ 31,945). Hepatic Impairment: In a study comparing the kinetics of pravastatin in patients with biopsy confirmed cirrhosis (N = 7) and normal subjects (N = 7), the mean AUC varied 18 fold in cirrhotic patients and 5 fold in healthy subjects. Similarly, the peak pravastatin values varied 47 fold for cirrhotic patients compared to 6 fold for healthy subjects [ see Warnings and Precautions ( 5.2 ) ]. Geriatric: In a single oral dose study using pravastatin 20 mg, the mean AUC for pravastatin was approximately 27% greater and the mean cumulative urinary excretion (CUE) approximately 19% lower in elderly men (65 to 75 years old) compared with younger men (19 to 31 years old). In a similar study conducted in women, the mean AUC for pravastatin was approximately 46% higher and the mean CUE approximately 18% lower in elderly women (65 to 78 years old) compared with younger women (18 to 38 years old). In both studies, C max , T max , and t ½ values were similar in older and younger subjects [ see Use in Specific Populations ( 8.5 ) ]. Pediatric: After 2 weeks of once-daily 20 mg oral pravastatin administration, the geometric means of AUC were 80.7 (CV 44%) and 44.8 (CV 89%) ng*hr/mL for children (8 to 11 years, N = 14) and adolescents (12 to 16 years, N = 10), respectively. The corresponding values for C max were 42.4 (CV 54%) and 18.6 ng/mL (CV 100%) for children and adolescents, respectively. No conclusion can be made based on these findings due to the small number of samples and large variability [ see Use in Specific Populations ( 8.4 ) ]. Drug-Drug Interactions Table 3: Effect of Coadministered Drugs on the Pharmacokinetics of Pravastatin Coadministered Drug and Dosing Regimen Pravastatin Dose (mg) Change in AUC Change in C max Cyclosporine 5 mg/kg single dose 40 mg single dose ↑282% ↑327% Clarithromycin 500 mg BID for 9 days 40 mg OD for 8 days ↑110% ↑128% Boceprevir 800 mg TID for 6 days 40 mg single dose ↑63% ↑49% Darunavir 600 mg BID/Ritonavir 100 mg BID for 7 days 40 mg single dose ↑81% ↑63% Colestipol 10 g single dose 20 mg single dose ↓47% ↓53% Cholestyramine 4 g single dose 20 mg single dose Administered simultaneously ↓40% ↓39% Administered 1 hour prior to cholestyramine ↑12% ↑30% Administered 4 hours after cholestyramine ↓12% ↓6.8% Cholestyramine 24 g OD for 4 weeks 20 mg BID for 8 weeks ↓51% ↑4.9% 5 mg BID for 8 weeks ↓38% ↑23% 10 mg BID for 8 weeks ↓18% ↓33% Fluconazole 200 mg IV for 6 days 20 mg PO + 10 mg IV ↓34% ↓33% 200 mg PO for 6 days 20 mg PO + 10 mg IV ↓16% ↓16% Kaletra 400 mg/100 mg BID for 14 days 20 mg OD for 4 days ↑33% ↑26% Verapamil IR 120 mg for 1 day and Verapamil ER 480 mg for 3 days 40 mg single dose ↑31% ↑42% Cimetidine 300 mg QID for 3 days 20 mg single dose ↑30% ↑9.8% Antacids 15 mL QID for 3 days 20 mg single dose ↓28% ↓24% Digoxin 0.2 mg OD for 9 days 20 mg OD for 9 days ↑23% ↑26% Probucol 500 mg single dose 20 mg single dose ↑14% ↑24% Warfarin 5 mg OD for 6 days 20 mg BID for 6 days ↓13% ↓6.7% Itraconazole 200 mg OD for 30 days 40 mg OD for 30 days ↑11% (compared to Day 1) ↑17% (compared to Day 1) Gemfibrozil 600 mg single dose 20 mg single dose ↓7% ↓20% Aspirin 324 mg single dose 20 mg single dose ↑4.7% ↑8.9% Niacin 1 g single dose 20 mg single dose ↓3.6% ↓8.2% Diltiazem 20 mg single dose ↑2.7% ↑30% Grapefruit juice 40 mg single dose ↓1.8% ↑3.7% BID = twice daily; OD = once daily; QID = four times daily Table 4: Effect of Pravastatin on the Pharmacokinetics of Coadministered Drugs Pravastatin Dosing Regimen Name and Dose Change in AUC Change in C max 20 mg BID for 6 days Warfarin 5 mg OD for 6 days ↑17% ↑15% Change in mean prothrombin time ↑0.4 sec 20 mg OD for 9 days Digoxin 0.2 mg OD for 9 days ↑4.6% ↑5.3% 20 mg BID for 4 weeks Antipyrine 1.2 g single dose ↑3% Not Reported 10 mg BID for 4 weeks ↑1.6% 5 mg BID for 4 weeks ↑ Less than 1% 20 mg OD for 4 days Kaletra 400 mg/100 mg BID for 14 days No change No change BID = twice daily; OD = once daily
| Cyclosporine 5 mg/kg single dose | 40 mg single dose | ↑282% | ↑327% |
| Clarithromycin 500 mg BID for 9 days | 40 mg OD for 8 days | ↑110% | ↑128% |
| Boceprevir 800 mg TID for 6 days | 40 mg single dose | ↑63% | ↑49% |
| Darunavir 600 mg BID/Ritonavir 100 mg BID for 7 days | 40 mg single dose | ↑81% | ↑63% |
| Colestipol 10 g single dose | 20 mg single dose | ↓47% | ↓53% |
| Cholestyramine 4 g single dose | 20 mg single dose | ||
| Administered simultaneously | ↓40% | ↓39% | |
| Administered 1 hour prior to cholestyramine | ↑12% | ↑30% | |
| Administered 4 hours after cholestyramine | ↓12% | ↓6.8% | |
| Cholestyramine 24 g OD for 4 weeks | 20 mg BID for 8 weeks | ↓51% | ↑4.9% |
| 5 mg BID for 8 weeks | ↓38% | ↑23% | |
| 10 mg BID for 8 weeks | ↓18% | ↓33% | |
| Fluconazole | |||
| 200 mg IV for 6 days | 20 mg PO + 10 mg IV | ↓34% | ↓33% |
| 200 mg PO for 6 days | 20 mg PO + 10 mg IV | ↓16% | ↓16% |
| Kaletra 400 mg/100 mg BID for 14 days | 20 mg OD for 4 days | ↑33% | ↑26% |
| Verapamil IR 120 mg for 1 day and Verapamil ER 480 mg for 3 days | 40 mg single dose | ↑31% | ↑42% |
| Cimetidine 300 mg QID for 3 days | 20 mg single dose | ↑30% | ↑9.8% |
| Antacids 15 mL QID for 3 days | 20 mg single dose | ↓28% | ↓24% |
| Digoxin 0.2 mg OD for 9 days | 20 mg OD for 9 days | ↑23% | ↑26% |
| Probucol 500 mg single dose | 20 mg single dose | ↑14% | ↑24% |
| Warfarin 5 mg OD for 6 days | 20 mg BID for 6 days | ↓13% | ↓6.7% |
| Itraconazole 200 mg OD for 30 days | 40 mg OD for 30 days | ↑11% (compared to Day 1) | ↑17% (compared to Day 1) |
| Gemfibrozil 600 mg single dose | 20 mg single dose | ↓7% | ↓20% |
| Aspirin 324 mg single dose | 20 mg single dose | ↑4.7% | ↑8.9% |
| Niacin 1 g single dose | 20 mg single dose | ↓3.6% | ↓8.2% |
| Diltiazem | 20 mg single dose | ↑2.7% | ↑30% |
| Grapefruit juice | 40 mg single dose | ↓1.8% | ↑3.7% |
| 20 mg BID for 6 days | Warfarin 5 mg OD for 6 days | ↑17% | ↑15% |
| Change in mean prothrombin time | ↑0.4 sec | ||
| 20 mg OD for 9 days | Digoxin 0.2 mg OD for 9 days | ↑4.6% | ↑5.3% |
| 20 mg BID for 4 weeks | Antipyrine 1.2 g single dose | ↑3% | Not Reported |
| 10 mg BID for 4 weeks | ↑1.6% | ||
| 5 mg BID for 4 weeks | ↑ Less than 1% | ||
| 20 mg OD for 4 days | Kaletra 400 mg/100 mg BID for 14 days | No change | No change |
Contraindications
Information about situations in which the drug product is contraindicated or should not be used because the risk of use clearly outweighs any possible benefit, including the type and nature of reactions that have been reported.4 CONTRAINDICATIONS Hypersensitivity to any component of this medication. ( 4.1 , 6.2 , 11 ) Active liver disease or unexplained, persistent elevations of serum transaminases. ( 4.2 , 5.2 ) Women who are pregnant or may become pregnant. ( 4.3 , 8.1 ) Nursing mothers. ( 4.4 , 8.3 ) 4.1 Hypersensitivity Hypersensitivity to any component of this medication. 4.2 Liver Active liver disease or unexplained, persistent elevations of serum transaminases [ see Warnings and Precautions ( 5.2 ) ]. 4.3 Pregnancy Atherosclerosis is a chronic process and discontinuation of lipid-lowering drugs during pregnancy should have little impact on the outcome of long-term therapy of primary hypercholesterolemia. Cholesterol and other products of cholesterol biosynthesis are essential components for fetal development (including synthesis of steroids and cell membranes). Since statins decrease cholesterol synthesis and possibly the synthesis of other biologically active substances derived from cholesterol, they are contraindicated during pregnancy and in nursing mothers. PRAVASTATIN SHOULD BE ADMINISTERED TO WOMEN OF CHILDBEARING AGE ONLY WHEN SUCH PATIENTS ARE HIGHLY UNLIKELY TO CONCEIVE AND HAVE BEEN INFORMED OF THE POTENTIAL HAZARDS. If the patient becomes pregnant while taking this class of drug, therapy should be discontinued immediately and the patient apprised of the potential hazard to the fetus [ see Use in Specific Populations ( 8.1 ) ]. 4.4 Nursing Mothers A small amount of pravastatin is excreted in human breast milk. Because statins have the potential for serious adverse reactions in nursing infants, women who require pravastatin sodium tablet treatment should not breastfeed their infants [s ee Use in Specific Populations ( 8.3 ) ].
Description
General information about the drug product, including the proprietary and established name of the drug, the type of dosage form and route of administration to which the label applies, qualitative and quantitative ingredient information, the pharmacologic or therapeutic class of the drug, and the chemical name and structural formula of the drug.11 DESCRIPTION Pravastatin sodium, USP is one of a class of lipid-lowering compounds, the statins, which reduce cholesterol biosynthesis. These agents are competitive inhibitors of HMG-CoA reductase, the enzyme catalyzing the early rate-limiting step in cholesterol biosynthesis, conversion of HMG-CoA to mevalonate. Pravastatin sodium, USP is designated chemically as 1-naphthaleneheptanoic acid, 1,2,6,7,8,8a-hexahydro-β,δ,6-trihydroxy-2-methyl-8-(2-methyl-1-oxobutoxy)-, monosodium salt, [1 S -[1α (β S *,δ S *),2α,6α,8β( R *),8aα]]-. It has the following structural formula: C 23 H 35 NaO 7 M.W. 446.52 Pravastatin sodium, USP is an odorless, white to off-white, fine or crystalline powder. It is a relatively polar hydrophilic compound with a partition coefficient (octanol/water) of 0.59 at a pH of 7. It is soluble in methanol and water (> 300 mg/mL), slightly soluble in isopropanol, and practically insoluble in acetone, acetonitrile, chloroform, and ether. Pravastatin Sodium Tablets USP are available for oral administration as 10 mg, 20 mg, and 40 mg tablets. Inactive ingredients include: calcium phosphate dibasic anhydrous, croscarmellose sodium, crospovidone, lactose anhydrous, microcrystalline cellulose, povidone and sodium stearyl fumarate. Additionally, the 10 mg tablet contains ferric oxide red; the 20 mg tablet contains ferric oxide yellow; and the 40 mg tablet contains FD&C Blue No. 1 Aluminum Lake and Yellow D&C No. 10; Also available for oral administration as 80 mg tablets. Inactive ingredients include: calcium phosphate dibasic, crospovidone, lactose anhydrous, microcrystalline cellulose, povidone and the 80 mg tablet contains magnesium stearate. Chemical Structure
Dosage and administration
Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.2 DOSAGE AND ADMINISTRATION Adults: the recommended starting dose is 40 mg once daily. Use 80 mg dose only for patients not reaching LDL-C goal with 40 mg. ( 2.2 ) Significant renal impairment: the recommended starting dose is 10 mg once daily. ( 2.2 ) Children (ages 8 to 13 years, inclusive): the recommended starting dose is 20 mg once daily. ( 2.3 ) Adolescents (ages 14 to 18 years): the recommended starting dose is 40 mg once daily. ( 2.3 ) 2.1 General Dosing Information The patient should be placed on a standard cholesterol-lowering diet before receiving pravastatin sodium tablets and should continue on this diet during treatment with pravastatin sodium tablets [see NCEP Treatment Guidelines for details on dietary therapy]. 2.2 Adult Patients The recommended starting dose is 40 mg once daily. If a daily dose of 40 mg does not achieve desired cholesterol levels, 80 mg once daily is recommended. In patients with significant renal impairment, a starting dose of 10 mg daily is recommended. Pravastatin sodium tablets can be administered orally as a single dose at any time of the day, with or without food. Since the maximal effect of a given dose is seen within 4 weeks, periodic lipid determinations should be performed at this time and dosage adjusted according to the patient’s response to therapy and established treatment guidelines. 2.3 Pediatric Patients Children (Ages 8 to 13 Years, Inclusive) The recommended dose is 20 mg once daily in children 8 to 13 years of age. Doses greater than 20 mg have not been studied in this patient population. Adolescents (Ages 14 to 18 Years) The recommended starting dose is 40 mg once daily in adolescents 14 to 18 years of age. Doses greater than 40 mg have not been studied in this patient population. Children and adolescents treated with pravastatin should be reevaluated in adulthood and appropriate changes made to their cholesterol-lowering regimen to achieve adult goals for LDL-C [ see Indications and Usage ( 1.2 ) ]. 2.4 Concomitant Lipid-Altering Therapy Pravastatin sodium tablets may be used with bile acid resins. When administering a bile-acid-binding resin (e.g., cholestyramine, colestipol) and pravastatin, pravastatin sodium tablets should be given either 1 hour or more before or at least 4 hours following the resin [ see Clinical Pharmacology ( 12.3 ) ]. 2.5 Dosage in Patients Taking Cyclosporine In patients taking immunosuppressive drugs such as cyclosporine concomitantly with pravastatin, therapy should begin with 10 mg of pravastatin sodium once-a-day at bedtime and titration to higher doses should be done with caution. Most patients treated with this combination received a maximum pravastatin sodium dose of 20 mg/day. In patients taking cyclosporine, therapy should be limited to 20 mg of pravastatin sodium once daily [ see Warnings and Precautions ( 5.1 ) and Drug Interactions ( 7.1 ) ]. 2.6 Dosage in Patients Taking Clarithromycin In patients taking clarithromycin, therapy should be limited to 40 mg of pravastatin sodium once daily [ see Drug Interactions ( 7.2 ) ].
Dosage forms and strengths
Information about all available dosage forms and strengths for the drug product to which the labeling applies. This field may contain descriptions of product appearance.3 DOSAGE FORMS AND STRENGTHS Pravastatin sodium tablets USP are supplied as: 10 mg tablets: Pink, unscored, round tablet, debossed “TEVA” on one side and “771” on the other side. 20 mg tablets : Light-yellow, unscored, round tablet, debossed “TEVA” on one side and “7201” on the other side. 40 mg tablets: Light-green, unscored, round tablet, debossed “TEVA” on one side and “7202” on the other side. 80 mg tablets : Off-white to mottled grey, unscored, oval-shaped tablet, debossed “TEVA” on one side and “7270” on the other side. Tablets: 10 mg, 20 mg, 40 mg, and 80 mg. ( 3 )
Indications and usage
A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.1 INDICATIONS AND USAGE Therapy with lipid-altering agents should be only one component of multiple risk factor intervention in individuals at significantly increased risk for atherosclerotic vascular disease due to hypercholesterolemia. Drug therapy is indicated as an adjunct to diet when the response to a diet restricted in saturated fat and cholesterol and other nonpharmacologic measures alone has been inadequate. Pravastatin Sodium Tablets USP are an HMG-CoA reductase inhibitor (statin) indicated as an adjunctive therapy to diet to: Reduce the risk of MI, revascularization, and cardiovascular mortality in hypercholesterolemic patients without clinically evident CHD. ( 1.1 ) Reduce elevated Total-C, LDL-C, ApoB, and TG levels and to increase HDL-C in patients with primary hypercholesterolemia and mixed dyslipidemia. ( 1.2 ) Reduce elevated serum TG levels in patients with hypertriglyceridemia. ( 1.2 ) Treat patients with primary dysbetalipoproteinemia who are not responding to diet. ( 1.2 ) Treat children and adolescent patients ages 8 years and older with heterozygous familial hypercholesterolemia after failing an adequate trial of diet therapy. ( 1.2 ) Limitations of use: Pravastatin Sodium Tablets USP have not been studied in Fredrickson Types I and V dyslipidemias. ( 1.3 ) 1.1 Prevention of Cardiovascular Disease In hypercholesterolemic patients without clinically evident coronary heart disease (CHD), Pravastatin Sodium Tablets USP are indicated to: reduce the risk of myocardial infarction (MI). reduce the risk of undergoing myocardial revascularization procedures. reduce the risk of cardiovascular mortality with no increase in death from non-cardiovascular causes. 1.2 Hyperlipidemia Pravastatin Sodium Tablets USP are indicated: as an adjunct to diet to reduce elevated total cholesterol (Total-C), low-density lipoprotein cholesterol (LDL-C), apolipoprotein B (ApoB), and triglyceride (TG) levels and to increase high-density lipoprotein cholesterol (HDL-C) in patients with primary hypercholesterolemia and mixed dyslipidemia ( Fredrickson Types IIa and IIb). 1 as an adjunct to diet for the treatment of patients with elevated serum TG levels ( Fredrickson Type IV). for the treatment of patients with primary dysbetalipoproteinemia ( Fredrickson Type III) who do not respond adequately to diet. as an adjunct to diet and lifestyle modification for treatment of heterozygous familial hypercholesterolemia (HeFH) in children and adolescent patients ages 8 years and older if after an adequate trial of diet the following findings are present: a. LDL-C remains ≥ 190 mg/dL or b. LDL-C remains ≥ 160 mg/dL and: there is a positive family history of premature cardiovascular disease (CVD) or two or more other CVD risk factors are present in the patient. 1.3 Limitations of Use Pravastatin Sodium Tablets USP have not been studied in conditions where the major lipoprotein abnormality is elevation of chylomicrons ( Fredrickson Types I and V).
Spl product data elements
Usually a list of ingredients in a drug product.Pravastatin Sodium Pravastatin Sodium PRAVASTATIN SODIUM PRAVASTATIN CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS CROSCARMELLOSE SODIUM CROSPOVIDONE ANHYDROUS LACTOSE CELLULOSE, MICROCRYSTALLINE POVIDONE K30 SODIUM STEARYL FUMARATE FD&C BLUE NO. 1 ALUMINUM OXIDE D&C YELLOW NO. 10 light-green TEVA;7202 Pravastatin Sodium Pravastatin Sodium PRAVASTATIN SODIUM PRAVASTATIN CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS CROSPOVIDONE ANHYDROUS LACTOSE CELLULOSE, MICROCRYSTALLINE POVIDONE K30 Magnesium Stearate off-white to mottled grey TEVA;7270 40mg 80mg
Animal pharmacology and or toxicology
Information from studies of the drug in animals, if the data were not relevant to nor included in other parts of the labeling. Most labels do not contain this field.13.2 Animal Toxicology and/or Pharmacology CNS Toxicity CNS vascular lesions, characterized by perivascular hemorrhage and edema and mononuclear cell infiltration of perivascular spaces, were seen in dogs treated with pravastatin at a dose of 25 mg/kg/day. These effects in dogs were observed at approximately 59 times the HD of 80 mg/day, based on AUC. Similar CNS vascular lesions have been observed with several other drugs in this class. A chemically similar drug in this class produced optic nerve degeneration (Wallerian degeneration of retinogeniculate fibers) in clinically normal dogs in a dose-dependent fashion starting at 60 mg/kg/day, a dose that produced mean plasma drug levels about 30 times higher than the mean drug level in humans taking the highest recommended dose (as measured by total enzyme inhibitory activity). This same drug also produced vestibulocochlear Wallerian-like degeneration and retinal ganglion cell chromatolysis in dogs treated for 14 weeks at 180 mg/kg/day, a dose which resulted in a mean plasma drug level similar to that seen with the 60 mg/kg/day dose. When administered to juvenile rats (postnatal days [PND] 4 through 80 at 5 to 45 mg/kg/day), no drug related changes were observed at 5 mg/kg/day. At 15 and 45 mg/kg/day, altered body-weight gain was observed during the dosing and 52 day recovery periods as well as slight thinning of the corpus callosum at the end of the recovery period. This finding was not evident in rats examined at the completion of the dosing period and was not associated with any inflammatory or degenerative changes in the brain. The biological relevance of the corpus callosum finding is uncertain due to the absence of any other microscopic changes in the brain or peripheral nervous tissue and because it occurred at the end of the recovery period. Neurobehavioral changes (enhanced acoustic startle responses and increased errors in water-maze learning) combined with evidence of generalized toxicity were noted at 45 mg/kg/day during the later part of the recovery period. Serum pravastatin levels at 15 mg/kg/day are approximately ≥ 1 times (AUC) the maximum pediatric dose of 40 mg. No thinning of the corpus callosum was observed in rats dosed with pravastatin (≥ 250 mg/kg/day) beginning PND 35 for 3 months suggesting increased sensitivity in younger rats. PND 35 in a rat is approximately equivalent to an 8 to 12-year-old human child. Juvenile male rats given 90 times (AUC) the 40 mg dose had decreased fertility (20%) with sperm abnormalities compared to controls.
Carcinogenesis and mutagenesis and impairment of fertility
Information about carcinogenic, mutagenic, or fertility impairment potential revealed by studies in animals. Information from human data about such potential is part of the warnings field.13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility In a 2 year study in rats fed pravastatin at doses of 10, 30, or 100 mg/kg body weight, there was an increased incidence of hepatocellular carcinomas in males at the highest dose (p < 0.01). These effects in rats were observed at approximately 12 times the human dose (HD) of 80 mg based on body surface area (mg/m 2 ) and at approximately 4 times the HD, based on AUC. In a 2 year study in mice fed pravastatin at doses of 250 and 500 mg/kg/day, there was an increased incidence of hepatocellular carcinomas in males and females at both 250 and 500 mg/kg/day (p < 0.0001). At these doses, lung adenomas in females were increased (p = 0.013). These effects in mice were observed at approximately 15 times (250 mg/kg/day) and 23 times (500 mg/kg/day) the HD of 80 mg, based on AUC. In another 2 year study in mice with doses up to 100 mg/kg/day (producing drug exposures approximately 2 times the HD of 80 mg, based on AUC), there were no drug-induced tumors. No evidence of mutagenicity was observed in vitro , with or without rat-liver metabolic activation, in the following studies: microbial mutagen tests, using mutant strains of Salmonella typhimurium or Escherichia coli ; a forward mutation assay in L5178Y TK +/− mouse lymphoma cells; a chromosomal aberration test in hamster cells; and a gene conversion assay using Saccharomyces cerevisiae . In addition, there was no evidence of mutagenicity in either a dominant lethal test in mice or a micronucleus test in mice. In a fertility study in adult rats with daily doses up to 500 mg/kg, pravastatin did not produce any adverse effects on fertility or general reproductive performance.
Nonclinical toxicology
Information about toxicology in non-human subjects.13 NONCLINICAL TOXICOLOGY 13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility In a 2 year study in rats fed pravastatin at doses of 10, 30, or 100 mg/kg body weight, there was an increased incidence of hepatocellular carcinomas in males at the highest dose (p < 0.01). These effects in rats were observed at approximately 12 times the human dose (HD) of 80 mg based on body surface area (mg/m 2 ) and at approximately 4 times the HD, based on AUC. In a 2 year study in mice fed pravastatin at doses of 250 and 500 mg/kg/day, there was an increased incidence of hepatocellular carcinomas in males and females at both 250 and 500 mg/kg/day (p < 0.0001). At these doses, lung adenomas in females were increased (p = 0.013). These effects in mice were observed at approximately 15 times (250 mg/kg/day) and 23 times (500 mg/kg/day) the HD of 80 mg, based on AUC. In another 2 year study in mice with doses up to 100 mg/kg/day (producing drug exposures approximately 2 times the HD of 80 mg, based on AUC), there were no drug-induced tumors. No evidence of mutagenicity was observed in vitro , with or without rat-liver metabolic activation, in the following studies: microbial mutagen tests, using mutant strains of Salmonella typhimurium or Escherichia coli ; a forward mutation assay in L5178Y TK +/− mouse lymphoma cells; a chromosomal aberration test in hamster cells; and a gene conversion assay using Saccharomyces cerevisiae . In addition, there was no evidence of mutagenicity in either a dominant lethal test in mice or a micronucleus test in mice. In a fertility study in adult rats with daily doses up to 500 mg/kg, pravastatin did not produce any adverse effects on fertility or general reproductive performance. 13.2 Animal Toxicology and/or Pharmacology CNS Toxicity CNS vascular lesions, characterized by perivascular hemorrhage and edema and mononuclear cell infiltration of perivascular spaces, were seen in dogs treated with pravastatin at a dose of 25 mg/kg/day. These effects in dogs were observed at approximately 59 times the HD of 80 mg/day, based on AUC. Similar CNS vascular lesions have been observed with several other drugs in this class. A chemically similar drug in this class produced optic nerve degeneration (Wallerian degeneration of retinogeniculate fibers) in clinically normal dogs in a dose-dependent fashion starting at 60 mg/kg/day, a dose that produced mean plasma drug levels about 30 times higher than the mean drug level in humans taking the highest recommended dose (as measured by total enzyme inhibitory activity). This same drug also produced vestibulocochlear Wallerian-like degeneration and retinal ganglion cell chromatolysis in dogs treated for 14 weeks at 180 mg/kg/day, a dose which resulted in a mean plasma drug level similar to that seen with the 60 mg/kg/day dose. When administered to juvenile rats (postnatal days [PND] 4 through 80 at 5 to 45 mg/kg/day), no drug related changes were observed at 5 mg/kg/day. At 15 and 45 mg/kg/day, altered body-weight gain was observed during the dosing and 52 day recovery periods as well as slight thinning of the corpus callosum at the end of the recovery period. This finding was not evident in rats examined at the completion of the dosing period and was not associated with any inflammatory or degenerative changes in the brain. The biological relevance of the corpus callosum finding is uncertain due to the absence of any other microscopic changes in the brain or peripheral nervous tissue and because it occurred at the end of the recovery period. Neurobehavioral changes (enhanced acoustic startle responses and increased errors in water-maze learning) combined with evidence of generalized toxicity were noted at 45 mg/kg/day during the later part of the recovery period. Serum pravastatin levels at 15 mg/kg/day are approximately ≥ 1 times (AUC) the maximum pediatric dose of 40 mg. No thinning of the corpus callosum was observed in rats dosed with pravastatin (≥ 250 mg/kg/day) beginning PND 35 for 3 months suggesting increased sensitivity in younger rats. PND 35 in a rat is approximately equivalent to an 8 to 12-year-old human child. Juvenile male rats given 90 times (AUC) the 40 mg dose had decreased fertility (20%) with sperm abnormalities compared to controls.
Package label principal display panel
The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.PACKAGE LABEL.PRINCIPAL DISPLAY PANEL NDC 43353-964-45 Pravastatin Sodium Tablets, USP 40 mg 45 Tablets Rx Only Each tablet contains 40 mg pravastatin sodium, USP. Usual Dosage: See package insert for full prescribing information. Store at 20° to 25°C (68° to 77°F) [See USP Controlled Room Temperature]. Protect from moisture. Protect from light. Dispense in a tight, light-resistant container as defined in the USP, with a child-resistant closure (as required). KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN. NDC 43353-966-45 Pravastatin Sodium Tablets, USP 80 mg 45 Tablets Rx Only Each tablet contains 80 mg pravastatin sodium, USP. Usual Dosage: See package insert for full prescribing information. Store at 20° to 25°C (68° to 77°F) [See USP Controlled Room Temperature]. Protect from moisture. Protect from light. Dispense in a tight, light-resistant container as defined in the USP, with a child-resistant closure (as required). KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN.
Spl unclassified section
Information not classified as belonging to one of the other fields. Approximately 40% of labeling with effective_time between June 2009 and August 2014 have information in this field.Repackaging Information Please reference the How Supplied section listed above for a description of individual tablets. This drug product has been received by Aphena Pharma - TN in a manufacturer or distributor packaged configuration and repackaged in full compliance with all applicable cGMP regulations. The package configurations available from Aphena are listed below: Count 40mg 45 43353-964-45 Count 80mg 45 43353-966-45 90 43353-966-60 Store between 20°-25°C (68°-77°F). See USP Controlled Room Temperature. Dispense in a tight light-resistant container as defined by USP. Keep this and all drugs out of the reach of children. Repackaged by: Cookeville, TN 38506 20160622DH Aphena Pharma Solutions - TN
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| 45 | 43353-964-45 |
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| 90 | 43353-966-60 |
Pravastatin Sodium: Information for patients
Information necessary for patients to use the drug safely and effectively, such as precautions concerning driving or the concomitant use of other substances that may have harmful additive effects.17 PATIENT COUNSELING INFORMATION Patients should be advised to report promptly unexplained muscle pain, tenderness or weakness, particularly if accompanied by malaise or fever or if these muscle signs or symptoms persist after discontinuing pravastatin sodium [ see Warnings and Precautions ( 5.1 ) ]. It is recommended that liver enzyme tests be performed before the initiation of pravastatin, and thereafter when clinically indicated. All patients treated with pravastatin should be advised to promptly report any symptoms that may indicate liver injury, including fatigue, anorexia, right upper abdominal discomfort, dark urine, or jaundice [ see Warnings and Precautions ( 5.2 ) ]. Manufactured For: AvKARE, Inc. Pulaski, TN 38478 Mfg. Rev. T 12/13 AV Rev. 09/14 (P)
Clinical studies
This field may contain references to clinical studies in place of detailed discussion in other sections of the labeling.14 CLINICAL STUDIES 14.1 Prevention of Coronary Heart Disease In the Pravastatin Primary Prevention Study (WOS), 3 the effect of pravastatin sodium on fatal and nonfatal CHD was assessed in 6595 men 45 to 64 years of age, without a previous MI, and with LDL-C levels between 156 to 254 mg/dL (4 to 6.7 mmol/L). In this randomized, double-blind, placebo-controlled study, patients were treated with standard care, including dietary advice, and either pravastatin 40 mg daily (N = 3302) or placebo (N = 3293) and followed for a median duration of 4.8 years. Median (25 th , 75 th percentile) percent changes from baseline after 6 months of pravastatin treatment in Total-C, LDL-C, TG, and HDL-C were −20.3 (−26.9, −11.7), −27.7 (−36, −16.9), −9.1 (−27.6, 12.5), and 6.7 (−2.1, 15.6), respectively. Pravastatin sodium significantly reduced the rate of first coronary events (either CHD death or nonfatal MI) by 31% (248 events in the placebo group [CHD death = 44, nonfatal MI = 204] versus 174 events in the pravastatin sodium group [CHD death = 31, nonfatal MI = 143], p = 0.0001 [see figure below]). The risk reduction with pravastatin sodium was similar and significant throughout the entire range of baseline LDL cholesterol levels. This reduction was also similar and significant across the age range studied with a 40% risk reduction for patients younger than 55 years and a 27% risk reduction for patients 55 years and older. The Pravastatin Primary Prevention Study included only men, and therefore it is not clear to what extent these data can be extrapolated to a similar population of female patients. Pravastatin sodium also significantly decreased the risk for undergoing myocardial revascularization procedures (coronary artery bypass graft [CABG] surgery or percutaneous transluminal coronary angioplasty [PTCA]) by 37% (80 vs 51 patients, p = 0.009) and coronary angiography by 31% (128 vs 90, p = 0.007). Cardiovascular deaths were decreased by 32% (73 vs 50, p = 0.03) and there was no increase in death from non-cardiovascular causes. 14.2 Secondary Prevention of Cardiovascular Events In the PLAC I 6 study, the effect of pravastatin therapy on coronary atherosclerosis was assessed by coronary angiography in patients with coronary disease and moderate hypercholesterolemia (baseline LDL-C range: 130 to 190 mg/dL). In this double-blind, multicenter, controlled clinical trial, angiograms were evaluated at baseline and at 3 years in 264 patients. Although the difference between pravastatin and placebo for the primary endpoint (per-patient change in mean coronary artery diameter) and 1 of 2 secondary endpoints (change in percent lumen diameter stenosis) did not reach statistical significance, for the secondary endpoint of change in minimum lumen diameter, statistically significant slowing of disease was seen in the pravastatin treatment group (p = 0.02). In the REGRESS 7 study, the effect of pravastatin on coronary atherosclerosis was assessed by coronary angiography in 885 patients with angina pectoris, angiographically documented coronary artery disease, and hypercholesterolemia (baseline total cholesterol range: 160 to 310 mg/dL). In this double-blind, multicenter, controlled clinical trial, angiograms were evaluated at baseline and at 2 years in 653 patients (323 treated with pravastatin). Progression of coronary atherosclerosis was significantly slowed in the pravastatin group as assessed by changes in mean segment diameter (p = 0.037) and minimum obstruction diameter (p = 0.001). Analysis of pooled events from PLAC I, PLAC II, 8 REGRESS, and KAPS 9 studies (combined N = 1891) showed that treatment with pravastatin was associated with a statistically significant reduction in the composite event rate of fatal and nonfatal MI (46 events or 6.4% for placebo versus 21 events or 2.4% for pravastatin, p = 0.001). The predominant effect of pravastatin was to reduce the rate of nonfatal MI. 14.3 Primary Hypercholesterolemia ( Fredrickson Types IIa and IIb) Pravastatin sodium is highly effective in reducing Total-C, LDL-C, and TG in patients with heterozygous familial, presumed familial combined, and non-familial (non-FH) forms of primary hypercholesterolemia, and mixed dyslipidemia. A therapeutic response is seen within 1 week, and the maximum response usually is achieved within 4 weeks. This response is maintained during extended periods of therapy. In addition, pravastatin sodium is effective in reducing the risk of acute coronary events in hypercholesterolemic patients with and without previous MI. A single daily dose is as effective as the same total daily dose given twice a day. In multicenter, double-blind, placebo-controlled studies of patients with primary hypercholesterolemia, treatment with pravastatin in daily doses ranging from 10 to 40 mg consistently and significantly decreased Total-C, LDL-C, TG, and Total-C/HDL-C and LDL-C/HDL-C ratios (see Table 7 ). In a pooled analysis of 2 multicenter, double-blind, placebo-controlled studies of patients with primary hypercholesterolemia, treatment with pravastatin at a daily dose of 80 mg (N = 277) significantly decreased Total-C, LDL-C, and TG. The 25 th and 75 th percentile changes from baseline in LDL-C for pravastatin 80 mg were −43% and −30%. The efficacy results of the individual studies were consistent with the pooled data (see Table 7 ). Treatment with pravastatin sodium modestly decreased VLDL-C and pravastatin sodium across all doses produced variable increases in HDL-C (see Table 7 ). Table 7: Primary Hypercholesterolemia Studies: Dose Response of Pravastatin Sodium Once Daily Administration Dose Total-C LDL-C HDL-C TG Mean Percent Changes From Baseline After 8 Weeks A multicenter, double-blind, placebo-controlled study. Placebo (N = 36) −3% −4% +1% −4% 10 mg (N = 18) −16% −22% +7% −15% 20 mg (N = 19) −24% −32% +2% −11% 40 mg (N = 18) −25% −34% +12% −24% Mean Percent Changes From Baseline After 6 Weeks Pooled analysis of 2 multicenter, double-blind, placebo-controlled studies. Placebo (N = 162) 0% −1% −1% +1% 80 mg (N = 277) −27% −37% +3% −19% In another clinical trial, patients treated with pravastatin in combination with cholestyramine (70% of patients were taking cholestyramine 20 or 24 g per day) had reductions equal to or greater than 50% in LDL-C. Furthermore, pravastatin attenuated cholestyramine-induced increases in TG levels (which are themselves of uncertain clinical significance). 14.4 Hypertriglyceridemia ( Fredrickson Type IV) The response to pravastatin in patients with Type IV hyperlipidemia (baseline TG > 200 mg/dL and LDL-C < 160 mg/dL) was evaluated in a subset of 429 patients. For pravastatin-treated subjects, the median (min, max) baseline TG level was 246 (200.5, 349.5) mg/dL (see Table 8 ). Table 8: Patients With Fredrickson Type IV Hyperlipidemia Median (25 th , 75 th Percentile) % Change From Baseline Pravastatin 40 mg (N = 429) Placebo (N = 430) TG −21.1 (−34.8, 1.3) −6.3 (−23.1, 18.3) Total-C −22.1 (−27.1, −14.8) 0.2 (−6.9, 6.8) LDL-C −31.7 (−39.6, −21.5) 0.7 (−9, 10) HDL-C 7.4 (−1.2, 17.7) 2.8 (−5.7, 11.7) Non-HDL-C −27.2 (−34, −18.5) −0.8 (−8.2, 7) 14.5 Dysbetalipoproteinemia ( Fredrickson Type III) The response to pravastatin in two double-blind crossover studies of 46 patients with genotype E2/E2 and Fredrickson Type III dysbetalipoproteinemia is shown in Table 9 . Table 9: Patients With Fredrickson Type III Dysbetalipoproteinemia Median (min, max) % Change From Baseline Median (min, max) at Baseline (mg/dL) Median % Change (min, max) Pravastatin 40 mg (N = 20) Study 1 Total-C 386.5 (245, 672) −32.7 (−58.5, 4.6) TG 443 (275, 1299) −23.7 (−68.5, 44.7) VLDL-C N = 14 206.5 (110, 379) −43.8 (−73.1, −14.3) LDL-C 117.5 (80, 170) −40.8 (−63.7, 4.6) HDL-C 30 (18, 88) 6.4 (−45, 105.6) Non-HDL-C 344.5 (215, 646) −36.7 (−66.3, 5.8) Median (min, max) at Baseline (mg/dL) Median % Change (min, max) Pravastatin 40 mg (N = 26) Study 2 Total-C 340.3 (230.1, 448.6) −31.4 (−54.5, −13) TG 343.2 (212.6, 845.9) −11.9 (−56.5, 44.8) VLDL-C 145 (71.5, 309.4) −35.7 (−74.7, 19.1) LDL-C 128.6 (63.8, 177.9) −30.3 (−52.2, 13.5) HDL-C 38.7 (27.1, 58) 5 (−17.7, 66.7) Non-HDL-C 295.8 (195.3, 421.5) −35.5 (−81, −13.5) 14.6 Pediatric Clinical Study A double-blind, placebo-controlled study in 214 patients (100 boys and 114 girls) with heterozygous familial hypercholesterolemia (HeFH), aged 8 to 18 years was conducted for 2 years. The children (aged 8 to 13 years) were randomized to placebo (N = 63) or 20 mg of pravastatin daily (N = 65) and the adolescents (aged 14 to 18 years) were randomized to placebo (N = 45) or 40 mg of pravastatin daily (N = 41). Inclusion in the study required an LDL-C level > 95 th percentile for age and sex and one parent with either a clinical or molecular diagnosis of familial hypercholesterolemia. The mean baseline LDL-C value was 239 mg/dL and 237 mg/dL in the pravastatin (range: 151 to 405 mg/dL) and placebo (range: 154 to 375 mg/dL) groups, respectively. Pravastatin significantly decreased plasma levels of LDL-C, Total-C, and ApoB in both children and adolescents (see Table 10 ). The effect of pravastatin treatment in the 2 age groups was similar. Table 10: Lipid-Lowering Effects of Pravastatin in Pediatric Patients With Heterozygous Familial Hypercholesterolemia: Least-Squares Mean % Change From Baseline at Month 24 (Last Observation Carried Forward: Intent-to-Treat) The above least-squares mean values were calculated based on log-transformed lipid values. Pravastatin 20 mg (Aged 8 to 13 years) N = 65 Pravastatin 40 mg (Aged 14 to 18 years) N = 41 Combined Pravastatin (Aged 8 to 18 years) N = 106 Combined Placebo (Aged 8 to 18 years) N = 108 95% CI of the Difference Between Combined Pravastatin and Placebo LDL-C −26.04 Significant at p ≤ 0.0001 when compared with placebo. −21.07 −24.07 −1.52 (−26.74, −18.86) TC −20.75 −13.08 −17.72 −0.65 (−20.40, −13.83) HDL-C 1.04 13.71 5.97 3.13 (−1.71, 7.43) TG −9.58 −0.30 −5.88 −3.27 (−13.95, 10.01) ApoB (N) −23.16 (61) −18.08 (39) −21.11 (100) −0.97 (106) (−24.29, −16.18) The mean achieved LDL-C was 186 mg/dL (range: 67 to 363 mg/dL) in the pravastatin group compared to 236 mg/dL (range: 105 to 438 mg/dL) in the placebo group. The safety and efficacy of pravastatin doses above 40 mg daily have not been studied in children. The long-term efficacy of pravastatin therapy in childhood to reduce morbidity and mortality in adulthood has not been established. Figure
| Mean Percent Changes From Baseline After 8 Weeks | ||||
| Placebo (N = 36) | −3% | −4% | +1% | −4% |
| 10 mg (N = 18) | −16% | −22% | +7% | −15% |
| 20 mg (N = 19) | −24% | −32% | +2% | −11% |
| 40 mg (N = 18) | −25% | −34% | +12% | −24% |
| Mean Percent Changes From Baseline After 6 Weeks | ||||
| Placebo (N = 162) | 0% | −1% | −1% | +1% |
| 80 mg (N = 277) | −27% | −37% | +3% | −19% |
| TG | −21.1 (−34.8, 1.3) | −6.3 (−23.1, 18.3) |
| Total-C | −22.1 (−27.1, −14.8) | 0.2 (−6.9, 6.8) |
| LDL-C | −31.7 (−39.6, −21.5) | 0.7 (−9, 10) |
| HDL-C | 7.4 (−1.2, 17.7) | 2.8 (−5.7, 11.7) |
| Non-HDL-C | −27.2 (−34, −18.5) | −0.8 (−8.2, 7) |
| Median (min, max) at Baseline (mg/dL) | Median % Change (min, max) Pravastatin 40 mg (N = 20) | |
| Total-C | 386.5 (245, 672) | −32.7 (−58.5, 4.6) |
| TG | 443 (275, 1299) | −23.7 (−68.5, 44.7) |
| VLDL-C | 206.5 (110, 379) | −43.8 (−73.1, −14.3) |
| LDL-C | 117.5 (80, 170) | −40.8 (−63.7, 4.6) |
| HDL-C | 30 (18, 88) | 6.4 (−45, 105.6) |
| Non-HDL-C | 344.5 (215, 646) | −36.7 (−66.3, 5.8) |
| Median (min, max) at Baseline (mg/dL) | Median % Change (min, max) Pravastatin 40 mg (N = 26) | |
| Total-C | 340.3 (230.1, 448.6) | −31.4 (−54.5, −13) |
| TG | 343.2 (212.6, 845.9) | −11.9 (−56.5, 44.8) |
| VLDL-C | 145 (71.5, 309.4) | −35.7 (−74.7, 19.1) |
| LDL-C | 128.6 (63.8, 177.9) | −30.3 (−52.2, 13.5) |
| HDL-C | 38.7 (27.1, 58) | 5 (−17.7, 66.7) |
| Non-HDL-C | 295.8 (195.3, 421.5) | −35.5 (−81, −13.5) |
| −26.04 | −21.07 | −24.07 | −1.52 | (−26.74, −18.86) | |
| −20.75 | −13.08 | −17.72 | −0.65 | (−20.40, −13.83) | |
| 1.04 | 13.71 | 5.97 | 3.13 | (−1.71, 7.43) | |
| −9.58 | −0.30 | −5.88 | −3.27 | (−13.95, 10.01) | |
| −23.16 | −18.08 | −21.11 | −0.97 (106) | (−24.29, −16.18) |
References
This field may contain references when prescription drug labeling must summarize or otherwise relay on a recommendation by an authoritative scientific body, or on a standardized methodology, scale, or technique, because the information is important to prescribing decisions.15 REFERENCES 1. Fredrickson DS, Levy RI, Lees RS. Fat transport in lipoproteins - An integrated approach to mechanisms and disorders. N Engl J Med. 1967;276: 34-44, 94-103, 148-156, 215-225, 273 -281. 2. Manson JM, Freyssinges C, Ducrocq MB, Stephenson WP. Postmarketing surveillance of lovastatin and simvastatin exposure during pregnancy. Reprod Toxicol. 1996;10(6):439-446. 3. Shepherd J, Cobbe SM, Ford I, et al, for the West of Scotland Coronary Prevention Study Group (WOS). Prevention of coronary heart disease with pravastatin in men with hypercholesterolemia. N Engl J Med. 1995;333:1301-1307. 6. Pitt B, Mancini GBJ, Ellis SG, et al, for the PLAC I Investigators. Pravastatin limitation of atherosclerosis in the coronary arteries (PLAC I): Reduction in atherosclerosis progression and clinical events. J Am Coll Cardiol. 1995;26:1133-1139. 7. Jukema JW, Bruschke AVG, van Boven AJ, et al, for the Regression Growth Evaluation Statin Study Group (REGRESS). Effects of lipid lowering by pravastatin on progression and regression of coronary artery disease in symptomatic man with normal to moderately elevated serum cholesterol levels. Circ. 1995;91:2528-2540. 8. Crouse JR, Byington RP, Bond MG, et al. Pravastatin, lipids, and atherosclerosis in the carotid arteries: Design features of a clinical trial with carotid atherosclerosis outcome (PLAC II). Control Clin Trials. 1992;13:495-506. 9. Salonen R, Nyyssonen K, Porkkala E, et al. Kuopio Atherosclerosis Prevention Study (KAPS). A population-based primary preventive trial of the effect of LDL lowering on atherosclerotic progression in carotid and femoral arteries. Circ. 1995;92:1758-1764.
Geriatric use
Information about any limitations on any geriatric indications, needs for specific monitoring, hazards associated with use of the drug in the geriatric population.8.5 Geriatric Use The beneficial effect of pravastatin in elderly subjects in reducing cardiovascular events and in modifying lipid profiles was similar to that seen in younger subjects. The adverse event profile in the elderly was similar to that in the overall population. Other reported clinical experience has not identified differences in responses to pravastatin between elderly and younger patients. Mean pravastatin AUCs are slightly (25% to 50%) higher in elderly subjects than in healthy young subjects, but mean maximum plasma concentration (C max ), time to maximum plasma concentration (T max ), and half-life (t ½ ) values are similar in both age groups and substantial accumulation of pravastatin would not be expected in the elderly [ see Clinical Pharmacology ( 12.3 ) ]. Since advanced age (≥ 65 years) is a predisposing factor for myopathy, pravastatin sodium should be prescribed with caution in the elderly [ see Warnings and Precautions ( 5.1 ) and Clinical Pharmacology ( 12.3 ) ].
Nursing mothers
Information about excretion of the drug in human milk and effects on the nursing infant, including pertinent adverse effects observed in animal offspring.8.3 Nursing Mothers A small amount of pravastatin is excreted in human breast milk. Because of the potential for serious adverse reactions in nursing infants, women taking pravastatin sodium should not nurse [ see Contraindications ( 4.4 ) ]. Pravastatin crosses the placenta and is found in fetal tissue at 30% maternal plasma levels following a single 20 mg/kg dose given to pregnant rats on gestation day 18. Similar studies in lactating rats indicate secretion of pravastatin into breast milk at 0.2 to 6.5 times higher levels than maternal plasma at exposures equivalent to 2 times human exposure at the MRHD.
Pediatric use
Information about any limitations on any pediatric indications, needs for specific monitoring, hazards associated with use of the drug in any subsets of the pediatric population (such as neonates, infants, children, or adolescents), differences between pediatric and adult responses to the drug, and other information related to the safe and effective pediatric use of the drug.8.4 Pediatric Use The safety and effectiveness of pravastatin sodium in children and adolescents from 8 to 18 years of age have been evaluated in a placebo-controlled study of 2 years duration. Patients treated with pravastatin had an adverse experience profile generally similar to that of patients treated with placebo with influenza and headache commonly reported in both treatment groups [ see Adverse Reactions ( 6.4 ) ]. Doses greater than 40 mg have not been studied in this population. Children and adolescent females of childbearing potential should be counseled on appropriate contraceptive methods while on pravastatin therapy [ see Contraindications ( 4.3 ) and Use in Specific Populations ( 8.1 ) ]. For dosing information [ see Dosage and Administration ( 2.3 ) ]. Double-blind, placebo-controlled pravastatin studies in children less than 8 years of age have not been conducted.
Pregnancy
Information about effects the drug may have on pregnant women or on a fetus. This field may be ommitted if the drug is not absorbed systemically and the drug is not known to have a potential for indirect harm to the fetus. It may contain information about the established pregnancy category classification for the drug. (That information is nominally listed in the teratogenic_effects field, but may be listed here instead.)8.1 Pregnancy Teratogenic Effects Pregnancy Category X [ See Contraindications ( 4.3 ). ] Safety in pregnant women has not been established. Available data in women inadvertently taking pravastatin while pregnant do not suggest any adverse clinical events. However, there are no adequate and well-controlled studies in pregnant women. Therefore, it is not known whether pravastatin can cause fetal harm when administered to a pregnant woman or can affect reproductive capacity. Pravastatin should be used during pregnancy only if the potential benefit outweighs the potential risk to the fetus and patients have been informed of the potential hazards. Rare reports of congenital anomalies have been received following intrauterine exposure to other statins. In a review 2 of approximately 100 prospectively followed pregnancies in women exposed to simvastatin or lovastatin, the incidences of congenital anomalies, spontaneous abortions, and fetal deaths/stillbirths did not exceed what would be expected in the general population. The number of cases is adequate to exclude a ≥ 3 to 4 fold increase in congenital anomalies over the background incidence. In 89% of the prospectively followed pregnancies, drug treatment was initiated prior to pregnancy and was discontinued at some point in the first trimester when pregnancy was identified. As safety in pregnant women has not been established and there is no apparent benefit to therapy with pravastatin sodium during pregnancy [ see Contraindications ( 4.3 ) ], treatment should be immediately discontinued as soon as pregnancy is recognized. Pravastatin sodium should be administered to women of childbearing potential only when such patients are highly unlikely to conceive and have been informed of the potential hazards. Pravastatin was neither embryolethal nor teratogenic in rats at doses up to 1000 mg/kg daily or in rabbits at doses of up to 50 mg/kg daily. These doses resulted in 10 times (rabbit) or 120 times (rat) the human exposure at 80 mg/day maximum recommended human dose (MRHD) based on surface area (mg/m 2 ). In pregnant rats given oral gavage doses of 4, 20, 100, 500, and 1000 mg/kg/day from gestation days 7 through 17 (organogenesis) increased mortality of offspring and skeletal anomalies were observed at 100 mg/kg/day systemic exposure, 10 times the human exposure at 80 mg/day MRHD based on body surface area (mg/m 2 ). In pregnant rats given oral gavage doses of 10, 100, and 1000 mg/kg/day from gestation day 17 through lactation day 21 (weaning) increased mortality of offspring and developmental delays were observed at 100 mg/kg/day systemic exposure, 12 times the human exposure at 80 mg/day MRHD based on body surface area (mg/m 2 ).
Use in specific populations
Information about use of the drug by patients in specific populations, including pregnant women and nursing mothers, pediatric patients, and geriatric patients.8 USE IN SPECIFIC POPULATIONS 8.1 Pregnancy Teratogenic Effects Pregnancy Category X [ See Contraindications ( 4.3 ). ] Safety in pregnant women has not been established. Available data in women inadvertently taking pravastatin while pregnant do not suggest any adverse clinical events. However, there are no adequate and well-controlled studies in pregnant women. Therefore, it is not known whether pravastatin can cause fetal harm when administered to a pregnant woman or can affect reproductive capacity. Pravastatin should be used during pregnancy only if the potential benefit outweighs the potential risk to the fetus and patients have been informed of the potential hazards. Rare reports of congenital anomalies have been received following intrauterine exposure to other statins. In a review 2 of approximately 100 prospectively followed pregnancies in women exposed to simvastatin or lovastatin, the incidences of congenital anomalies, spontaneous abortions, and fetal deaths/stillbirths did not exceed what would be expected in the general population. The number of cases is adequate to exclude a ≥ 3 to 4 fold increase in congenital anomalies over the background incidence. In 89% of the prospectively followed pregnancies, drug treatment was initiated prior to pregnancy and was discontinued at some point in the first trimester when pregnancy was identified. As safety in pregnant women has not been established and there is no apparent benefit to therapy with pravastatin sodium during pregnancy [ see Contraindications ( 4.3 ) ], treatment should be immediately discontinued as soon as pregnancy is recognized. Pravastatin sodium should be administered to women of childbearing potential only when such patients are highly unlikely to conceive and have been informed of the potential hazards. Pravastatin was neither embryolethal nor teratogenic in rats at doses up to 1000 mg/kg daily or in rabbits at doses of up to 50 mg/kg daily. These doses resulted in 10 times (rabbit) or 120 times (rat) the human exposure at 80 mg/day maximum recommended human dose (MRHD) based on surface area (mg/m 2 ). In pregnant rats given oral gavage doses of 4, 20, 100, 500, and 1000 mg/kg/day from gestation days 7 through 17 (organogenesis) increased mortality of offspring and skeletal anomalies were observed at 100 mg/kg/day systemic exposure, 10 times the human exposure at 80 mg/day MRHD based on body surface area (mg/m 2 ). In pregnant rats given oral gavage doses of 10, 100, and 1000 mg/kg/day from gestation day 17 through lactation day 21 (weaning) increased mortality of offspring and developmental delays were observed at 100 mg/kg/day systemic exposure, 12 times the human exposure at 80 mg/day MRHD based on body surface area (mg/m 2 ). 8.3 Nursing Mothers A small amount of pravastatin is excreted in human breast milk. Because of the potential for serious adverse reactions in nursing infants, women taking pravastatin sodium should not nurse [ see Contraindications ( 4.4 ) ]. Pravastatin crosses the placenta and is found in fetal tissue at 30% maternal plasma levels following a single 20 mg/kg dose given to pregnant rats on gestation day 18. Similar studies in lactating rats indicate secretion of pravastatin into breast milk at 0.2 to 6.5 times higher levels than maternal plasma at exposures equivalent to 2 times human exposure at the MRHD. 8.4 Pediatric Use The safety and effectiveness of pravastatin sodium in children and adolescents from 8 to 18 years of age have been evaluated in a placebo-controlled study of 2 years duration. Patients treated with pravastatin had an adverse experience profile generally similar to that of patients treated with placebo with influenza and headache commonly reported in both treatment groups [ see Adverse Reactions ( 6.4 ) ]. Doses greater than 40 mg have not been studied in this population. Children and adolescent females of childbearing potential should be counseled on appropriate contraceptive methods while on pravastatin therapy [ see Contraindications ( 4.3 ) and Use in Specific Populations ( 8.1 ) ]. For dosing information [ see Dosage and Administration ( 2.3 ) ]. Double-blind, placebo-controlled pravastatin studies in children less than 8 years of age have not been conducted. 8.5 Geriatric Use The beneficial effect of pravastatin in elderly subjects in reducing cardiovascular events and in modifying lipid profiles was similar to that seen in younger subjects. The adverse event profile in the elderly was similar to that in the overall population. Other reported clinical experience has not identified differences in responses to pravastatin between elderly and younger patients. Mean pravastatin AUCs are slightly (25% to 50%) higher in elderly subjects than in healthy young subjects, but mean maximum plasma concentration (C max ), time to maximum plasma concentration (T max ), and half-life (t ½ ) values are similar in both age groups and substantial accumulation of pravastatin would not be expected in the elderly [ see Clinical Pharmacology ( 12.3 ) ]. Since advanced age (≥ 65 years) is a predisposing factor for myopathy, pravastatin sodium should be prescribed with caution in the elderly [ see Warnings and Precautions ( 5.1 ) and Clinical Pharmacology ( 12.3 ) ]. 8.6 Homozygous Familial Hypercholesterolemia Pravastatin has not been evaluated in patients with rare homozygous familial hypercholesterolemia. In this group of patients, it has been reported that statins are less effective because the patients lack functional LDL receptors.
How supplied
Information about the available dosage forms to which the labeling applies, and for which the manufacturer or distributor is responsible. This field ordinarily includes the strength of the dosage form (in metric units), the units in which the dosage form is available for prescribing, appropriate information to facilitate identification of the dosage forms (such as shape, color, coating, scoring, and National Drug Code), and special handling and storage condition information.16 HOW SUPPLIED/STORAGE AND HANDLING 16.1 How Supplied Pravastatin Sodium Tablets USP are supplied as: 10 mg tablets: Pink, unscored, round tablet, debossed “TEVA” on one side and “771” on the other side in bottles of 90 (NDC 665-90) and 1000 (NDC 42291-665-10). 20 mg tablets : Light-yellow, unscored, round tablet, debossed “TEVA” on one side and “7201” on the other side in bottles of 90 (NDC 42291-667-90) and 1000 (NDC 42291-667-10). 40 mg tablets: Light-green, unscored, round tablet, debossed “TEVA” on one side and “7202” on the other side in bottles of 90 (NDC 42291-668-90)and (NDC 42291-668-10) 1000. 80 mg tablets: Off-white to mottled grey, unscored, oval-shaped tablet, debossed “TEVA” on one side and “7270” on the other side in bottles of 45 (NDC 42291-669-45) ,90 (NDC 42291-669-90) and 1000 (NDC 42291-669-10). 16.2 Storage Store at 20° to 25°C (68° to 77°F) [See USP Controlled Room Temperature]. Keep tightly closed (protect from moisture). Protect from light. Dispense in a tight, light-resistant container as defined in the USP, with a child-resistant closure (as required). KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN.
Storage and handling
Information about safe storage and handling of the drug product.16.2 Storage Store at 20° to 25°C (68° to 77°F) [See USP Controlled Room Temperature]. Keep tightly closed (protect from moisture). Protect from light. Dispense in a tight, light-resistant container as defined in the USP, with a child-resistant closure (as required). KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN.
Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API