🇺🇸 mercaptopurine tablet in United States
10 US adverse-event reports
Safety signals — FAERS
Adverse reaction reports describe suspected side effects. A report does not mean the drug caused the event — co-medications, underlying disease and coincidence all contribute.
- Window: 23 April 2025 – 23 April 2026
- Total reports: 10
Most-reported reactions
- Acute Lymphocytic Leukaemia Recurrent — 1 report (10%)
- Alanine Aminotransferase Increased — 1 report (10%)
- Anger — 1 report (10%)
- Anxiety — 1 report (10%)
- Aspartate Aminotransferase Increased — 1 report (10%)
- Blood Bilirubin Increased — 1 report (10%)
- Blood Lactate Dehydrogenase Increased — 1 report (10%)
- Central Nervous System Leukaemia — 1 report (10%)
- Cerebral Haemorrhage — 1 report (10%)
- Condition Aggravated — 1 report (10%)
Other Oncology approved in United States
Frequently asked questions
Is mercaptopurine tablet approved in United States?
mercaptopurine tablet does not currently have US marketing authorisation in our dataset.
Who is the marketing authorisation holder for mercaptopurine tablet in United States?
National Cancer Institute (NCI) is the originator. The local marketing authorisation holder may differ — check the official source linked above.