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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does AZATHIOPRINE Cause Joint dislocation? 502 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 502 reports of Joint dislocation have been filed in association with AZATHIOPRINE (AZATHIOPRINE). This represents 1.5% of all adverse event reports for AZATHIOPRINE.

502
Reports of Joint dislocation with AZATHIOPRINE
1.5%
of all AZATHIOPRINE reports
279
Deaths
167
Hospitalizations

How Dangerous Is Joint dislocation From AZATHIOPRINE?

Of the 502 reports, 279 (55.6%) resulted in death, 167 (33.3%) required hospitalization, and 159 (31.7%) were considered life-threatening.

Is Joint dislocation Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for AZATHIOPRINE. However, 502 reports have been filed with the FAERS database.

What Other Side Effects Does AZATHIOPRINE Cause?

Drug ineffective (8,076) Off label use (5,358) Drug intolerance (3,392) Condition aggravated (2,832) Rheumatoid arthritis (2,746) Treatment failure (2,483) Arthralgia (2,427) Drug hypersensitivity (2,421) Nausea (2,178) Pneumonia (2,157)

What Other Drugs Cause Joint dislocation?

ADALIMUMAB (1,549) ETANERCEPT (802) METHOTREXATE (792) TOFACITINIB (685) ABATACEPT (656) TOCILIZUMAB (646) CERTOLIZUMAB PEGOL (577) GOLIMUMAB (572) RITUXIMAB (557) DICLOFENAC (536)

Which AZATHIOPRINE Alternatives Have Lower Joint dislocation Risk?

AZATHIOPRINE vs AZD-1222 AZATHIOPRINE vs AZELAIC ACID AZATHIOPRINE vs AZELASTINE AZATHIOPRINE vs AZELASTINE\FLUTICASONE AZATHIOPRINE vs AZELNIDIPINE

Related Pages

AZATHIOPRINE Full Profile All Joint dislocation Reports All Drugs Causing Joint dislocation AZATHIOPRINE Demographics