from the market because of risks to the patients. Usually this has been prompted by unexpected adverse effects that were not detected during Phase III
data from the wider patient community.
| Drug name
| Withdrawn
| Remarks |
| Thalidomide
| 1950s–1960s
| Withdrawn because of risk of teratogenicity; returned to market for use in leprosy and multiple myeloma under FDA orphan drug rules |
| Lysergic acid diethylamide (LSD)
| 1950s–1960s
| Marketed as a psychiatric cure-all; withdrawn after it became widely used recreationally |
| Diethylstilbestrol
| 1970s
| Withdrawn because of risk of teratogenicity |
| Phenformin and Buformin
| 1978
| Withdrawn because of risk of lactic acidosis |
| Ticrynafen
| 1982
| Withdrawn because of risk of hepatitis |
| Zimelidine
| 1983
| Withdrawn worldwide because of risk of Guillain-Barré syndrome |
| Methaqualone
| 1984
| Withdrawn because of risk of addiction and overdose. |
| Triazolam
| 1991
| Withdrawn in the United Kingdom because of risk of psychiatric adverse drug reactions. This drug continues to be available in the U.S. |
| Temafloxacin
| 1992
| Withdrawn in the United States because of allergic reactions and cases of hemolytic anemia, leading to three patient deaths. |
| Alpidem (Ananxyl)
| 1996
| Withdrawn because of rare but serious hepatotoxicity. |
| Fen-phen (popular combination of fenfluramine and phentermine)
| 1997
| Phentermine remains on the market, dexfenfluramine and fenfluramine – later withdrawn as caused heart valve disorder |
| Tolrestat (Alredase)
| 1997
| Withdrawn because of risk of severe hepatotoxicity |
| Terfenadine (Seldane)
| 1998
| Withdrawn because of risk of cardiac arrhythmias; superseded by fexofenadine |
| Mibefradil (Posicor)
| 1998
| Withdrawn because of dangerous interactions with other drugs |
| Temazepam (Restoril, Euhypnos, Normison, Remestan, Tenox, Norkotral)
| 1999
| Withdrawn in Sweden and Norway because of diversion, abuse, and a relatively high rate of overdose deaths in comparison to other drugs of its group. This drug continues to be available in the U.S. |
| Astemizole (Hismanal)
| 1999
| Arrhythmias because of interactions with other drugs |
| Troglitazone (Rezulin)
| 2000
| Withdrawn because of risk of hepatotoxicity; superseded by pioglitazone and rosiglitazone |
| Alosetron (Lotronex)
| 2000
| Withdrawn because of risk of fatal complications of constipation; reintroduced 2002 on a restricted basis |
| Cisapride (Propulsid)
| 2000s
| Withdrawn in many countries because of risk of cardiac arrhythmias |
| Amineptine (Survector)
| 2000
| Withdrawn because of hepatotoxicity, dermatological side effects, and abuse potential. |
| Phenylpropanolamine (Propagest, Dexatrim)
| 2000
| Withdrawn because of risk of stroke in women under 50 years of age when taken at high doses (75mg twice daily) for weight loss. |
| Trovafloxacin (Trovan)
| 2001
| Withdrawn because of risk of liver failure |
| cerivastatin (Baycol, Lipobay)
| 2001
| Withdrawn because of risk of rhabdomyolysis |
| Rapacuronium (Raplon)
| 2001
| Withdrawn in many countries because of risk of fatal bronchospasm |
| Rofecoxib (Vioxx)
| 2004
| Withdrawn because of risk of myocardial infarction |
| mixed amphetamine salts (Adderall XR)
| 2005
| Withdrawn in Canada because of risk of stroke. See Health Canada press release |
| hydromorphone extended-release (Palladone)
| 2005
| Withdrawn because of a high risk of accidental overdose when administered with alcohol |
| Pemoline (Cylert)
| 2005
| Withdrawn from U.S. market because of hepatotoxicity |
| Natalizumab (Tysabri)
| 2005-2006
| Voluntarily withdrawn from U.S. market because of risk of Progressive multifocal leukoencephalopathy (PML). Returned to market July, 2006. |
| Ximelagatran (Exanta)
| 2006
| Withdrawn because of risk of hepatotoxicity (liver damage). |
| Tegaserod (Zelnorm)
| 2007
| Withdrawn because of imbalance of cardiovascular ischemic events, including heart attack and stroke. |
| Aprotinin (Trasylol)
| 2007
| Withdrawn because of increased risk of complications or death; permanently withdrawn in 2008 except for research use |
| Lumiracoxib
| 2007-2008
| Progressively withdrawn around the world because of serious side effects, mainly liver damage |
Has a list of U.S. withdrawals through 2005