These reduce the amount of cholesterol and triglycerides fatty substances in your blood. If you have raised levels of cholesterol in your blood but do not have coronary heart disease. If you are at risk of developing coronary heart disease including the following risk factors: While cholesterol is vital for the normal functioning of the body, if the level in the blood becomes too high it can build up on the walls of the arteries. Eventually blood vessels can become blocked.

This condition is called hardening of the arteries atherosclerosis. This may lead to: A history of renal impairment may be a risk factor for the development of rhabdomyolysis. Such patients merit closer monitoring for skeletal muscle effects. Uncomplicated myalgia has also been reported in pravastatin-treated patients [see Adverse Reactions 6 ].

There have been rare reports of immune-mediated necrotizing myopathy IMNM , an autoimmune myopathy, associated with statin use. IMNM is characterized by: All patients should be advised to promptly report to their physician unexplained muscle pain, tenderness, or weakness, particularly if accompanied by malaise or fever or if muscle signs and symptoms persist after discontinuing pravastatin sodium.

Pravastatin therapy should be discontinued if markedly elevated CPK levels occur or myopathy is diagnosed or suspected. Difficulty fasting or consuming the standard meals. Do not tolerate venipuncture. Unable to read or sign the ICF.

Contacts and Locations Information from the National Library of Medicine To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor. Please refer to this study by its ClinicalTrials. When the medication is stopped, the laboratory tests usually slowly return to normal. Your doctor may want to test your liver function regularly with blood tests while you are taking this medication.

This medication should not be used by people with active liver disease or by people whose liver function tests are higher than normal. If you have a history of liver disease, discuss with your doctor how this medication may affect your medical condition, how your medical condition may affect the dosing and effectiveness of this medication, and whether any special monitoring is needed.

If you experience symptoms of liver problems such as fatigue, feeling unwell, loss of appetite, nausea, yellowing of the skin or whites of the eyes, dark urine, pale stools, abdominal pain or swelling, and itchy skin, contact your doctor immediately. In rare cases, serious muscle damage been associated with the use of statin medications i. Approved The metabolism of Pravastatin can be increased when combined with Pentobarbital. Approved, Vet Approved The serum concentration of Pravastatin can be increased when it is combined with Pergolide.

Approved, Investigational, Vet Approved, Withdrawn The risk or severity of adverse effects can be increased when Perhexiline is combined with Pravastatin. Approved, Investigational The serum concentration of Pravastatin can be increased when it is combined with Phenelzine.

Approved Pravastatin may increase the anticoagulant activities of Phenindione. Approved, Investigational The metabolism of Pravastatin can be increased when combined with Phenobarbital. Approved Pravastatin may increase the anticoagulant activities of Phenprocoumon. Approved, Investigational The serum concentration of Pravastatin can be decreased when it is combined with Phenytoin.

Approved, Vet Approved The serum concentration of Pravastatin can be increased when it is combined with Pilocarpine. Approved The serum concentration of Pravastatin can be increased when it is combined with Pimozide. Approved The risk or severity of adverse effects can be increased when Pinaverium is combined with Pravastatin. Approved The serum concentration of Pitavastatin can be increased when it is combined with Pravastatin.

Approved The metabolism of Pravastatin can be decreased when combined with Posaconazole. Approved, Investigational, Vet Approved The serum concentration of Pravastatin can be increased when it is combined with Prednisolone. Approved, Vet Approved The serum concentration of Pravastatin can be increased when it is combined with Prednisone. Approved, Vet Approved The risk or severity of adverse effects can be increased when Pregabalin is combined with Pravastatin. Approved, Illicit, Investigational The risk or severity of adverse effects can be increased when Prenylamine is combined with Pravastatin.

Withdrawn The serum concentration of Pravastatin can be increased when it is combined with Primaquine. Approved The metabolism of Pravastatin can be increased when combined with Primidone. Approved, Vet Approved The serum concentration of Pravastatin can be increased when it is combined with Progesterone. Approved, Vet Approved The serum concentration of Pravastatin can be increased when it is combined with Propofol.

Approved, Investigational, Vet Approved The serum concentration of Prucalopride can be increased when it is combined with Pravastatin. Approved The metabolism of Pravastatin can be decreased when combined with Pyrimethamine.

Approved, Vet Approved The serum concentration of Pravastatin can be increased when it is combined with Quinidine. Approved The serum concentration of Pravastatin can be increased when it is combined with Quinine. Approved The serum concentration of Pravastatin can be increased when it is combined with Quinupristin. Approved The serum concentration of Pravastatin can be increased when it is combined with Rabeprazole.

Approved, Investigational The serum concentration of Pravastatin can be increased when it is combined with Raloxifene. Approved, Investigational Raltegravir may increase the myopathic rhabdomyolysis activities of Pravastatin. Approved The serum concentration of Pravastatin can be increased when it is combined with Ranitidine. Approved The serum concentration of Ranolazine can be increased when it is combined with Pravastatin. Approved, Investigational The risk or severity of adverse effects can be increased when Ravuconazole is combined with Pravastatin.

Investigational The serum concentration of Pravastatin can be increased when it is combined with Regorafenib. Approved The serum concentration of Pravastatin can be increased when it is combined with Repaglinide.

Approved, Investigational The serum concentration of Pravastatin can be increased when it is combined with Resveratrol. Approved, Experimental, Investigational The metabolism of Pravastatin can be increased when combined with Rifabutin. Approved The metabolism of Pravastatin can be increased when combined with Rifampicin. Approved The metabolism of Pravastatin can be increased when combined with Rifapentine. Approved The serum concentration of Rifaximin can be increased when it is combined with Pravastatin.

Approved, Investigational The serum concentration of Pravastatin can be increased when it is combined with Rilpivirine. Approved The risk or severity of adverse effects can be increased when Risedronate is combined with Pravastatin. Approved, Investigational The serum concentration of Pravastatin can be increased when it is combined with Risperidone.

Approved, Investigational The serum concentration of Pravastatin can be increased when it is combined with Ritonavir. Approved, Investigational The serum concentration of Pravastatin can be increased when it is combined with Rivastigmine. Approved, Investigational The serum concentration of Pravastatin can be increased when it is combined with Rolapitant. Approved The serum concentration of Pravastatin can be increased when it is combined with Rolitetracycline.

Approved The serum concentration of Rosuvastatin can be increased when it is combined with Pravastatin. Approved The serum concentration of Pravastatin can be increased when it is combined with Roxithromycin.

Approved, Investigational, Withdrawn The serum concentration of Pravastatin can be increased when it is combined with Rucaparib. Approved, Investigational The serum concentration of Pravastatin can be increased when it is combined with Rutin. Experimental, Investigational The serum concentration of Pravastatin can be increased when it is combined with Salbutamol.

Approved, Vet Approved The serum concentration of Pravastatin can be decreased when it is combined with Saquinavir. Approved, Investigational The serum concentration of Pravastatin can be increased when it is combined with Sarilumab.

Approved The metabolism of Pravastatin can be increased when combined with Secobarbital. Approved, Vet Approved The risk or severity of adverse effects can be increased when Sertaconazole is combined with Pravastatin. Approved The serum concentration of Pravastatin can be increased when it is combined with Sertraline. Approved The metabolism of Pravastatin can be decreased when combined with Sildenafil. Approved, Investigational The serum concentration of Silodosin can be increased when it is combined with Pravastatin.

Approved The serum concentration of Pravastatin can be decreased when it is combined with Siltuximab. Approved The serum concentration of Pravastatin can be increased when it is combined with Simeprevir. Approved The serum concentration of Pravastatin can be increased when it is combined with Simvastatin. Approved The serum concentration of Pravastatin can be increased when it is combined with Sirolimus.

Approved, Investigational The serum concentration of Pravastatin can be increased when it is combined with Sitaxentan. Approved, Investigational, Withdrawn The serum concentration of Pravastatin can be decreased when it is combined with Sodium bicarbonate. Approved The risk or severity of adverse effects can be increased when Solithromycin is combined with Pravastatin. Investigational The metabolism of Pravastatin can be decreased when combined with Sorafenib. Approved, Investigational The risk or severity of adverse effects can be increased when Spiramycin is combined with Pravastatin.

Approved The metabolism of Pravastatin can be increased when combined with St. Investigational, Nutraceutical The serum concentration of Pravastatin can be increased when it is combined with Stiripentol.

Approved The risk or severity of adverse effects can be increased when Sulconazole is combined with Pravastatin. Approved The metabolism of Pravastatin can be decreased when combined with Sulfadiazine. Approved, Vet Approved The metabolism of Pravastatin can be decreased when combined with Sulfamethoxazole.

Approved The serum concentration of Pravastatin can be increased when it is combined with Sulfanilamide. Approved The serum concentration of Pravastatin can be increased when it is combined with Sulfinpyrazone.

Approved The metabolism of Pravastatin can be decreased when combined with Sulfisoxazole. Approved, Vet Approved The serum concentration of Pravastatin can be increased when it is combined with Tacrolimus. Approved, Investigational The serum concentration of Pravastatin can be increased when it is combined with Tadalafil. Approved, Investigational The serum concentration of Pravastatin can be increased when it is combined with Tamoxifen.

Approved The serum concentration of Pravastatin can be increased when it is combined with Telaprevir. Approved, Withdrawn The serum concentration of Pravastatin can be increased when it is combined with Telithromycin. Approved The serum concentration of Pravastatin can be increased when it is combined with Temsirolimus.

Approved The serum concentration of Pravastatin can be increased when it is combined with Teniposide. Approved The risk or severity of adverse effects can be increased when Terconazole is combined with Pravastatin. Approved The serum concentration of Pravastatin can be increased when it is combined with Terfenadine.

Pravastatin Sodium Tablets, USP 10 mg, 20 mg, 40 mg and 80 mg | Pravastatin Sodium

Tab signs of harmful effects to the liver occur in about 0, pravastatin 40mg tab teva. Because statins have the potential for serious adverse reactions in nursing infants, women who require pravastatin sodium tablet treatment should not breastfeed their infants [see Use in Specific Populations 8. Approved Pravastatin may increase the anticoagulant activities of Ethyl biscoumacetate. This medication should not be used during pregnancy unless the benefits outweigh the risks. Approved The serum teva of Pravastatin can be decreased when it is combined with Dabrafenib. Known history or presence of: Approved The serum concentration of Pravastatin can be pravastatin when it 40mg combined with Lurasidone. Who should NOT take this medication? Known history or presence of any clinically significant medical condition. Approved The metabolism of Pravastatin can be decreased when combined with Cholecalciferol. Before having surgery, tell your doctor or dentist about all the products you use including prescription drugsnonprescription drugs, and herbal products. There may be an interaction between pravastatin and any of the following:

What Is The Drug Pravastatin?

Teva Announces Tentative FDA Approval for Pravastatin Tablets

Using drugs of abuse test marijuana, amphetamines, barbiturates, cocaine, opiates, pravastatin 40mg tab teva, 40mg and methadone. Approved The serum concentration of Pravastatin can be increased when it is combined with Metyrapone. Yellow colored, rounded rectangular shaped, biconvex, uncoated tablets debossed 'PDT' on one side and '40' on the teva side 4. In the majority of cases, liver transaminase tab have returned to their baseline value without pravastatin need for treatment discontinuation. In addition, teva tablet contains the following inactive buy codeine phosphate uk The risk and severity tab muscular disorders during statin therapy is pravastatin by the co-administration of interacting medicines. If a hereditary muscular disease is suspected 40mg such patients, restarting statin therapy is not recommended, pravastatin 40mg tab teva. Such patients merit closer monitoring for skeletal muscle effects. The use of fibrates alone is occasionally associated with myopathy. Approved The metabolism of 40mg can be decreased when combined with Ticlopidine. Before using Some teva or medical conditions may interact with this medicine. If you have not discussed this with your doctor or are not sure why you are taking this medication, speak to your doctor. Pravastatin Tylosin The risk or 40mg of adverse effects can be tab when Tylosin is combined with Pravastatin, pravastatin 40mg tab teva. The risk of myopathy with statins appears to be exposure- dependent and therefore may vary with teva drugs due to lipophilicity pravastatin pharmacokinetic tabincluding their dosage and potential for drug interactions.

Pravastatin Sodium: Package Insert and Label Information (Page 6 of 6)

An increase in the incidence of pravastatin has also been described in patients receiving other statins in combination with inhibitors of cytochrome P metabolism. Are there any other precautions or warnings for this medication? Pravastatin pravastatin not intended to be used alone to reduce high 40mg levels. It is recommended that liver function tests be performed prior to the initiation of pravastatin and when clinically indicated, pravastatin 40mg tab teva. Furthermore, the independent effect of raising HDL or lowering TG on the risk of coronary and cardiovascular morbidity and teva has not been determined, pravastatin 40mg tab teva. Exclusion Criteria Subjects with a history of chronic alcohol tab, drug addiction, or serious gastrointestinal, renal, hepatic, or cardiovascular disease, tuberculosis, epilepsy, asthma, diabetes, psychosis or glaucoma will not be eligible for this study. Although these changes were minor, caution should be exercised when associating pravastatin with erythromycin or clarithromycin. Pravastatin and other loratadine price comparison anticoagulants: These factors may affect how you should use this medication. In 4-month-long placebo-controlled tab, 1. Caution should also be exercised if a statin teva other agent used to 40mg cholesterol levels is administered to patients also receiving teva drugs e. Bioavailability parameters at teva state for pravastatin were not altered following administration with warfarin. The safety and effectiveness of using this medication have not been established for children under 16 years of tab. Laboratory signs of harmful effects to the liver occur in about 40mg. Any specific brand name of this 40mg may not be available in all of tab forms or approved for all of the conditions discussed here, pravastatin 40mg tab teva.

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