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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 Post procedural complication? 56 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 56 reports of Post procedural complication have been filed in association with AZATHIOPRINE (AZATHIOPRINE). This represents 0.2% of all adverse event reports for AZATHIOPRINE.

56
Reports of Post procedural complication with AZATHIOPRINE
0.2%
of all AZATHIOPRINE reports
1
Deaths
14
Hospitalizations

How Dangerous Is Post procedural complication From AZATHIOPRINE?

Of the 56 reports, 1 (1.8%) resulted in death, 14 (25.0%) required hospitalization, and 1 (1.8%) were considered life-threatening.

Is Post procedural complication Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for AZATHIOPRINE. However, 56 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 Post procedural complication?

ADALIMUMAB (2,494) ETANERCEPT (318) CALCIUM\DEXTROSE\MAGNESIUM\SODIUM\SODIUM (244) UPADACITINIB (241) RISANKIZUMAB-RZAA (232) INFLIXIMAB (217) METHOTREXATE (188) TREPROSTINIL (174) HUMAN IMMUNOGLOBULIN G (159) PREDNISONE (157)

Which AZATHIOPRINE Alternatives Have Lower Post procedural complication 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 Post procedural complication Reports All Drugs Causing Post procedural complication AZATHIOPRINE Demographics