Atorvastatin FDA Alerts

The FDA Alerts below may be specifically about atorvastatin or relate to a group or class of drugs which include atorvastatin.

MedWatch Safety Alerts are distributed by the FDA and published by Drugs.com. Following is a list of possible medication recalls, market withdrawals, alerts and warnings.

Recent FDA Alerts for atorvastatin

FDA Requests Removal of Strongest Warning Against Using Cholesterol-Lowering Statins During Pregnancy; Still Advises Most Pregnant Patients Should Stop Taking Statins

Jul 20, 2021 | Audience:  Patient, Health Professional, Pharmacy 

What safety information is FDA announcing?

The U.S. Food and Drug Administration (FDA) is requesting removal of its strongest warning against using cholesterol-lowering statin medicines in pregnant patients. Despite the change, most patients should stop statins once they learn they are pregnant. We have conducted a comprehensive review of all available data and are requesting that statin manufacturers make this change to the prescribing information as part of FDA’s ongoing effort to update the pregnancy and breastfeeding information for all prescription medicines.

Patients should not breastfeed when taking a statin because the medicine may pass into breast milk and pose a risk to the baby. Many can stop statins temporarily until breastfeeding ends. However, patients requiring ongoing statin treatment should not breastfeed and instead use infant formula or other alternatives.

What is FDA doing?

We are requesting revisions to the information about use in pregnancy in the prescribing information of the entire class of statin medicines. These changes include removing the contraindication against using these medicines in all pregnant patients. A contraindication is FDA’s strongest warning and is only added when a medicine should not be used because the risk clearly outweighs any possible benefit. Because the benefits of statins may include prevention of serious or potentially fatal events in a small group of very high-risk pregnant patients, contraindicating these drugs in all pregnant women is not appropriate.

FDA expects removing the contraindication will enable health care professionals and patients to make individual decisions about benefit and risk, especially for those at very high risk of heart attack or stroke. This includes patients with homozygous familial hypercholesterolemia and those who have previously had a heart attack or stroke. Statins are safe to use in patients who are not pregnant but may become pregnant.

What are statins and how can they help me?

Statins are a class of prescription medicines that have been used for decades to lower low-density lipoprotein (LDL-C or “bad”) cholesterol in the blood. Statins work by reducing the amount of cholesterol made by the liver and helping the liver remove cholesterol already in the blood. Statins also can lower the risk for heart attack and stroke in those who have heart disease or risk factors for it. These medicines may help stabilize the plaques that can build up inside blood vessel walls, which can interfere with blood flow to the heart and brain, leading to heart attack and stroke.

Medicines in the statin class include atorvastatin, fluvastatin, lovastatin, pitavastatin, pravastatin, rosuvastatin, and simvastatin. They are marketed as single-ingredient products and in combination with other medicines (See FDA-Approved Statin Medicines below). They are available as brand-name and generic products.

What should patients do?

Patients taking statins should notify your health care professionals if you become pregnant or suspect you are pregnant. Your health care professional will be able to advise whether you should stop taking the medicine during pregnancy and whether you may stop your statin temporarily while breastfeeding. Patients who are at high risk of heart attack or stroke who require statins after giving birth should not breastfeed and should use alternatives such as infant formula.

What should health care professionals do?

Health care professionals should discontinue statin therapy in most pregnant patients, or they can consider the ongoing therapeutic needs of the individual patient, particularly those at very high risk for cardiovascular events during pregnancy. Because of the chronic nature of cardiovascular disease, treatment of hyperlipidemia is not generally necessary during pregnancy. Discuss with patients whether they may discontinue statins temporarily while breastfeeding. Advise those who require a statin because of their cardiovascular risk that breastfeeding is not recommended because the medicine may pass into breast milk.

We hope the revised language in the prescribing information will help reassure health care professionals that statins are safe to prescribe in patients who can become pregnant, and help them reassure patients with unintended statin exposure in early pregnancy or before pregnancy is recognized that the medicine is unlikely to harm the unborn baby.

What did FDA review?

When FDA approved the first statin in 1987, the medicine came with our strongest warning recommending against use during pregnancy and breastfeeding. This was based on several factors. These were safety signals from animal data at drug exposures higher than human doses, potential concern that lowering cholesterol may negatively affect the unborn baby or infant, and the perspective that short-term use during pregnancy and breastfeeding did not provide a substantial benefit to the mother. All statins approved subsequently have carried the same warning.

Since then, multiple randomized trials and meta-analyses have demonstrated the benefit of statin therapy on the prevention of cardiovascular events. In addition, data from published observational studies of statin use in pregnant women have not identified a drug-associated risk of major birth defects when controlling for other risks such as diabetes and are insufficient to determine if there is a drug-associated risk of miscarriage.1-15 Overall, animal data suggest limited potential of statins to cause birth defects or miscarriage and limited potential to affect nervous system development in an unborn baby. However, because statins decrease the body’s ability to make cholesterol and possibly other substances, it is possible these medicines could harm an unborn baby when taken by a pregnant mother (See Data Summary for more details).

How do I report side effects from statins?

To help FDA track safety issues with medicines, we urge patients and health care professionals to report side effects involving statins or other medicines to the FDA MedWatch program, using the information in the “Contact FDA” box at the bottom of the page.

How can I get new safety information on medicines I’m prescribing or taking?

You can sign up for email alerts Disclaimer about Drug Safety Communications on medicines or medical specialties of interest to you.

FDA-Approved Statin Medicines

Brand Name	Active Ingredient(s)
Lipitor	atorvastatin
Caduet	atorvastatin and amlodipine
Lescol XL	fluvastatin
Altoprev	lovastatin
Livalo	pitavastatin
Zypitamag	pitavastatin
Pravachol	pravastatin
Crestor	rosuvastatin
Ezallor Sprinkle	rosuvastatin
Roszet	rosuvastatin and ezetimibe
Zocor	simvastatin
Flolipid	simvastatin
Vytorin	simvastatin and ezetimibe

Facts about Statins

Statins are a class of medicines used to lower cholesterol in the blood. Statins work by reducing the amount of cholesterol made by the liver and by helping the liver remove cholesterol already in the blood.
Statins also can lower the risk for heart attack and stroke in patients who have heart disease or risk factors for it. These medicines may help stabilize the plaques that can build up inside blood vessel walls, which can interfere with blood flow to the heart and brain, leading to heart attack and stroke.
Common side effects of statins include headache, nausea, muscle pain, diarrhea, and constipation.

Additional Information for Patients

FDA is requesting that manufacturers of cholesterol-lowering statins remove FDA’s strongest warning in the current prescribing information, which states that statins should never be used in patients during pregnancy. However, most patients should still stop statins once they learn they are pregnant.
Inform your health care professional if you become pregnant or suspect you are pregnant while taking a statin medicine. Your health care professional will be able to advise whether you should stop taking the medicine.
Statins are safe to use if you are not pregnant but can become pregnant. If you are taking a statin before you know you are pregnant, it is unlikely to harm your unborn baby.
Discuss with your health care professional if you are breastfeeding or plan to do so. Breastfeeding is not recommended in patients taking a statin. Your health care professional can help you determine whether it will be better for you to stop the statin temporarily while breastfeeding or whether you need to continue taking it and so should not breastfeed. If ongoing statin treatment is necessary, infant formula and other alternatives are available.
Always consult with your health care professional about the use of all medicines during pregnancy or while breastfeeding.
Talk to your health care professional if you have any questions or concerns about your statin medicine.
To help FDA track safety issues with medicines, report side effects from statins or other medicines to the FDA MedWatch program, using the information in the "Contact FDA" box at the bottom of this page.
You can sign up for email alerts about Drug Safety Communications on medicines or medical specialties of interest to you.

Additional Information for Health Care Professionals

FDA is requesting that manufacturers of cholesterol-lowering statins remove the contraindication included in the current prescribing information stating these medicines should never be used in patients during pregnancy.
Health care professionals should discontinue statin therapy in most pregnant patients. Alternatively, health care professionals should consider the ongoing therapeutic needs of the individual patient, especially patients at very high risk of cardiovascular events during pregnancy, such as patients with homozygous familial hypercholesterolemia or those with established cardiovascular disease.
Statins are safe to prescribe in patients who are not pregnant but may become pregnant. Reassure patients who have an unintended exposure to statins in early pregnancy that it is unlikely to cause harm to the developing fetus.
Treatment of hyperlipidemia is not generally necessary during pregnancy. Atherosclerosis is a chronic process and the temporary discontinuation of lipid-lowering drugs during pregnancy should have little impact on the outcome of long-term therapy of primary hyperlipidemia for most patients.
There is insufficient evidence to determine whether statins can cause miscarriage.
Observational studies have not identified an increase in birth defects associated with statin use during pregnancy after adjusting for potential confounders.
Animal data suggest limited potential for statins to cause malformations, and limited potential to affect the developing nervous system or cause embryofetal death. Nevertheless, statins decrease the synthesis of cholesterol and possibly other biologically active substances derived from cholesterol. Therefore, statins may cause fetal harm when administered to pregnant patients. Counsel pregnant women of this potential risk.
Some statins have been shown to pass into human milk and may cause harm to the breastfed infant based on the mechanism of action.
Advise patients who can become pregnant to inform their health care professionals of a known or suspected pregnancy, or if they are breastfeeding or plan to do so, to discuss whether their statin should be discontinued.
To help FDA track safety issues with medicines, report adverse events involving statins or other medicines to the FDA MedWatch program, using the information in the "Contact Us" box at the bottom of this page.
You can sign up for email alerts about Drug Safety Communications on medicines or medical specialties of interest to you.

Data Summary

FDA reviewed data from case series and prospective and retrospective observational cohort studies over decades of use of statins in pregnant women.1-15 Multiple larger, well-designed, and controlled observational studies did not find an increase in major birth defects associated with use of statins during pregnancy. The most recent 2015 Medicaid cohort linkage study of 1,152 statin-exposed pregnant women compared to 886,996 controls did not find a significant teratogenic effect from maternal use of statins in the first trimester of pregnancy, after adjusting for potential confounders.2 Propensity score-based methods were used to control for maternal age, diabetes, hypertension, obesity, and alcohol and tobacco use. The relative risk of congenital malformations between the group with statin use and the group with no statin use in the first trimester was 1.07 (95% confidence interval (CI) 0.85 to 1.37) after controlling for confounders, particularly pre-existing diabetes. There were also no statistically significant increases in any of the organ-specific malformations assessed after accounting for confounders. In the majority of pregnancies, statin treatment was initiated prior to pregnancy and was discontinued at some point in the first trimester when pregnancy was identified. Study limitations included reliance on physician coding to define the presence of a malformation, lack of control for certain confounders such as body mass index, use of prescription dispensing as verification for the use of a statin, and lack of information on non-live births.

Published data from prospective and retrospective observational cohort studies with statin use in pregnant women are insufficient to determine if there is a drug-associated risk of miscarriage. Many older studies did not report or discuss the rate of miscarriage; however, three studies included miscarriage in their analyses and did not find an increased risk once adjustments were made for confounders.3, 9, 10 In 2009, McGrogan et al.8 reported an adjusted risk ratio for terminations of 2.48 (95% CI 1.65-3.73). However, this study did not differentiate between elective terminations and miscarriage, and an increased rate of elective terminations would be expected in a study of pregnant women exposed to a drug contraindicated during pregnancy. In a meta-analysis of six small observational studies of statin exposure in pregnant women, Zarek et al.4 reported a risk ratio of miscarriage of 1.35 (95% CI 1.04-1.75). However, many of the studies included in the analysis, which were older and included the McGrogan 2009 study, did not control for multiple confounders that are known to increase the risk of miscarriage. In 2017, McGrogan et al.1 published a retrospective cohort study specifically looking at fetal loss as a primary outcome. The authors compared 281 statin-exposed pregnant women versus 2,643 controls. The cohorts were matched for maternal age, diabetes mellitus, hypertension and body mass index, and free text was used to help identify type of loss (i.e., miscarriage vs. elective termination). They found a miscarriage rate of 25% in statin-exposed versus 21% for controls. The adjusted hazard ratio was 1.64 (95% CI 1.1-2.46). Although there was an attempt to control for the presence of diabetes, the authors acknowledged there might still be some confounding because the study was not controlled for the type or severity of diabetes, which can influence rate of miscarriage. They also acknowledged the possibility of residual misclassification regarding smoking and alcohol use based on changed behavior patterns during pregnancy.

FDA also re-reviewed nonclinical data from statin development programs. The totality of the data suggests a limited potential for statins to cause malformations or embryofetal lethality, and limited potential to affect nervous system development during human embryofetal development and during the pre- and post-natal period.

References

McGrogan A, Snowball J, Charlton RA. Statins during pregnancy: a cohort study using the General Practice Research Database to investigate pregnancy loss. Pharmacoepidemiol Drug Saf 2017;26:843-52.
Bateman BT, Hernandez-Diaz S, Fischer MA, Seely EW, Ecker JL, Franklin JM, et al. Statins and congenital malformations: cohort study. BMJ 2015;350:h1035.
Winterfeld U, Allignol A, Panchaud A, Rothuizen LE, Merlob P, Cuppers-Maarschalkerweerd B, et al. Pregnancy outcome following maternal exposure to statins: a multi-centre prospective study. BJOG 2013;120:463-71.
Zarek J, Delano KE, Nickel C, Laskin CA, Koren G. Are statins teratogenic in humans? Addressing the safety of statins in light of potential benefits during pregnancy. Expert Rev Obstet Gynecol 2013;8:513-24.
Schir E et al. Safety of statins in pregnancy. Société Française de Pharmacologie et de Thérapeutique Abstracts 2012; 26(Suppl 1):106.
Toleikyte I, Retterstøl K, Leren TP, Iversen PO. Pregnancy outcomes in familial hypercholesterolemia: a registry-based study. Circulation 2011;124:1606-14.
Colvin L, Slack-Smith L, Stanley FJ, Bower C. Linking a pharmaceutical claims database with a birth defects registry to investigate birth defect rates of suspected teratogens. Pharmacoepidemiol Drug Saf 2010;19:1137-50.
McGrogan A, Snowball J, de Vries CS. Statins and pregnancy outcomes: A cohort study in the GPRD. Pharmacoepidemiol Drug Saf 2009;18(Suppl 18):S75-6.
Paulus WE et al. Statin treatment in hypercholesterolemic mothers during early pregnancy. Geburtshilfe Und Frauenheilkunde 2008;68:S130.
Taguchi N, Rubin ET, Hosokawa A, Choi J, Ying AY, Moretti ME, et al. Prenatal exposure to HMG-CoA reductase inhibitors: effects on fetal and neonatal outcomes. Reprod Toxicol 2008;26:175-7.
Petersen EE, Mitchell AA, Carey JC, Werler MM, Louik C, Rasmussen SA, the National Birth Defects Prevention Study. Maternal exposure to statins and risk for birth defects: A case‐series approach. Am J Med Genet Part A 2008;146A:2701-5.
Ofori B, Rey E, Bérard A. Risk of congenital anomalies in pregnant users of statin drugs. Br J Clin Pharmacol 2007 Oct;64:496-509.
Pollack PS, Shields KE, Burnett DM, Osborne MJ, Cunningham ML, Stepanavage ME. Pregnancy outcomes after maternal exposure to simvastatin and lovastatin. Birth Defects Res A Clin Mol Teratol 2005;73:888-96.
Edison RJ, Muenke M. Mechanistic and epidemiologic considerations in the evaluation of adverse birth outcomes following gestational exposure to statins. Am J Med Genet A 2004;131:287-98.
Manson JM, Freyssinges C, Ducrocq MB, Stephenson WP. Postmarketing surveillance of lovastatin and simvastatin exposure during pregnancy. Reprod Toxicol 1996;10:439-46.

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Source: FDA

Atorvastatin Calcium Tablets by Ranbaxy Inc.: Recall - Presence of Foreign Substance

Nov 28, 2012 | Audience: Pharmacy, Patient, Health Professional

ISSUE: On November 9, 2012, Ranbaxy Inc. initiated a voluntary recall of 41 affected lots of Atorvastatin Calcium Tablets (10 mg, 20 mg and 40 mg) which is a solid oral dosage form, to the retail level. The Company is taking this voluntary action as a precautionary measure due to the fact that we cannot exclude the possibility that the affected lots may contain very small glass particles resembling a fine grain of sand (less than 1 mm in size). Because of the size of the particles which may be present in the affected lots it is unlikely to cause a significant safety concern. However, the possibility of adverse experiences arising primarily due to physical irritation cannot be ruled out.

BACKGROUND: The product is used to lower blood cholesterol and is packaged in plastic bottles, as 90 and 500 tablets per bottle. The affected lots of Atorvastatin Calcium Tablets and their respective NDC code, expiration date information can be found in the Firm Press Release. The recall does not affect or relate to the 80 mg dosage strength of Atorvastatin Calcium Tablets.

RECOMMENDATION: Consumers should immediately contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.

Healthcare professionals and patients are encouraged to report adverse events or side effects related to the use of these products to the FDA's MedWatch Safety Information and Adverse Event Reporting Program:

Complete and submit the report Online: www.accessdata.fda.gov/scripts/medwatch/index.cfm
Download form or call 1-800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178.

[11/28/2012 - Firm Press Release - Ranbaxy Inc.]

Statin Drugs - Drug Safety Communication: Class Labeling Change

Feb 28, 2012 | Audience: Cardiology, Family Practice, Patients

ISSUE: FDA has approved important safety label changes for the class of cholesterol-lowering drugs known as statins. The changes include removal of routine monitoring of liver enzymes from drug labels. Information about the potential for generally non-serious and reversible cognitive side effects and reports of increased blood sugar and glycosylated hemoglobin (HbA1c) levels has been added to the statin labels.

The lovastatin label has been extensively updated with new contraindications and dose limitations when it is taken with certain medicines that can increase the risk for muscle injury.

Read the FDA Drug Safety Communication for more information.

BACKGROUND: Statins are a class of prescription drugs used together with diet and exercise to reduce blood levels of low-density lipoprotein (LDL) cholesterol (“bad cholesterol”). Marketed as single-ingredient products, including Lipitor (atorvastatin), Lescol (fluvastatin), Mevacor (lovastatin), Altoprev (lovastatin extended-release), Livalo (pitavastatin), Pravachol (pravastatin), Crestor (rosuvastatin), and Zocor (simvastatin). Also marketed as combination products, including Advicor (lovastatin/niacin extended-release), Simcor (simvastatin/niacin extended-release),and Vytorin (simvastatin/ezetimibe).

RECOMMENDATION: Healthcare professionals should perform liver enzyme tests before initiating statin therapy in patients and as clinically indicated thereafter. If serious liver injury with clinical symptoms and/or hyperbilirubinemia or jaundice occurs during treatment, therapy should be interrupted. If an alternate etiology is not found, the statin should not be restarted.

Healthcare professionals should follow the recommendations in the lovastatin label regarding drugs that may increase the risk of myopathy/rhabdomyolysis when used with lovastatin.

Complete and submit the report Online: www.accessdata.fda.gov/scripts/medwatch/index.cfm
Download form or call 1-800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178

[02/28/2012 - Drug Safety Communication - FDA]
[02/28/2012 - Consumer Update - FDA]

Statin drugs and amyotrophic lateral sclerosis (ALS)

Sep 30, 2008 | Audience: Neurologists, cardiologists, consumers[Posted 09/30/2008] An FDA analysis provides new evidence that the use of statins does not increase incidence of amyotrophic lateral sclerosis (ALS), a neurodegenerative disease often referred to as "Lou Gehrig's Disease." The FDA analysis, undertaken after the agency received a higher than expected number of reports of ALS in patients on statins, is based on data from 41 long-term controlled clinical trials. The results showed no increased incidence of the disease in patients treated with a statin compared with placebo.

The FDA is anticipating the completion of a case-control or epidemiological study of ALS and statin use. Results from this study should be available within 6-9 months. FDA is also examining the feasibility of conducting additional epidemiologic studies to examine the incidence and clinical course of ALS in patients taking statins.

Based on currently available information, health care professionals should not change their prescribing practices for statins and patients should not change their use of statins.

[September 29, 2008 - News Release - FDA]

Counterfeit "Lipitor" Sold in the United Kingdom

Aug 2, 2005 | Audience: Consumers and healthcare professionals[Posted 08/02/2005] FDA alerted U.S. residents to the recent recall of a batch of counterfeit "Lipitor" (atorvastatin) sold in the United Kingdom (U.K.). The medicine is used to treat high cholesterol. The counterfeit Lipitor 20mg tablets were recalled in the U.K. on July 28, 2005. Health authorities in the U.K. stated that initial results of tests performed on the counterfeit drugs do not indicate that this product poses an immediate risk to patients. Some U.S. residents may have obtained prescription drugs from the U.K. through on-line or storefront operations that do not supply legitimate, FDA-approved products, or through state-run drug importation programs that facilitate the purchase of unapproved foreign drugs. Consumers who purchase drugs through these arrangements may have received these counterfeit products. U.S. patients who have the identified U.K. drugs should stop using them and should consult their physician or pharmacist if they have any questions or concerns.

Counterfeit Drugs Purchased in Mexico

May 11, 2005 | Audience: Healthcare professionals and consumersThe FDA warned the public about the sale of counterfeit versions of Lipitor, Viagra, and an unapproved product promoted as "generic Evista" to U.S. consumers at pharmacies in Mexican border towns. The "generic Evista" was analyzed by FDA in coordination with the National Association of Boards of Pharmacy and was found to contain no active ingredient. The counterfeit Lipitor and counterfeit Viagra were analyzed by Pfizer, Inc. and were also found to contain no active ingredient. Consumers who have any of these counterfeit products should not use them and should contact their healthcare provider immediately.

[May 10, 2005 - Talk Paper - FDA]