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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 Hyperammonaemia? 11 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Hyperammonaemia have been filed in association with AZATHIOPRINE (AZATHIOPRINE). This represents 0.0% of all adverse event reports for AZATHIOPRINE.

11
Reports of Hyperammonaemia with AZATHIOPRINE
0.0%
of all AZATHIOPRINE reports
5
Deaths
5
Hospitalizations

How Dangerous Is Hyperammonaemia From AZATHIOPRINE?

Of the 11 reports, 5 (45.5%) resulted in death, 5 (45.5%) required hospitalization, and 4 (36.4%) were considered life-threatening.

Is Hyperammonaemia Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for AZATHIOPRINE. However, 11 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 Hyperammonaemia?

VALPROIC ACID (581) VALPROATE (328) FLUOROURACIL (263) DIVALPROEX (256) LEVETIRACETAM (192) TACROLIMUS (181) ACETAMINOPHEN (177) OXALIPLATIN (160) TOPIRAMATE (156) GLYCEROL PHENYLBUTYRATE (147)

Which AZATHIOPRINE Alternatives Have Lower Hyperammonaemia 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 Hyperammonaemia Reports All Drugs Causing Hyperammonaemia AZATHIOPRINE Demographics