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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 AMISULPRIDE Cause Condition aggravated? 140 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 140 reports of Condition aggravated have been filed in association with AMISULPRIDE (Barhemsys). This represents 4.4% of all adverse event reports for AMISULPRIDE.

140
Reports of Condition aggravated with AMISULPRIDE
4.4%
of all AMISULPRIDE reports
0
Deaths
73
Hospitalizations

How Dangerous Is Condition aggravated From AMISULPRIDE?

Of the 140 reports, 73 (52.1%) required hospitalization, and 7 (5.0%) were considered life-threatening.

Is Condition aggravated Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for AMISULPRIDE. However, 140 reports have been filed with the FAERS database.

What Other Side Effects Does AMISULPRIDE Cause?

Drug ineffective (665) Weight increased (346) Toxicity to various agents (305) Suicide attempt (261) Akathisia (252) Extrapyramidal disorder (226) Drug abuse (219) Leukopenia (218) Therapeutic product effect incomplete (200) Off label use (191)

What Other Drugs Cause Condition aggravated?

TOFACITINIB (16,925) INFLIXIMAB (16,616) DUPILUMAB (16,459) ETANERCEPT (15,897) METHOTREXATE (14,938) ADALIMUMAB (13,527) PREDNISONE (10,751) INFLIXIMAB-DYYB (10,275) HYDROXYCHLOROQUINE (8,848) RITUXIMAB (8,627)

Which AMISULPRIDE Alternatives Have Lower Condition aggravated Risk?

AMISULPRIDE vs AMITRIPTYLINE AMISULPRIDE vs AMITRIPTYLINE\PERPHENAZINE AMISULPRIDE vs AMIVANTAMAB AMISULPRIDE vs AMIVANTAMAB-VMJW AMISULPRIDE vs AMLODIPINE

Related Pages

AMISULPRIDE Full Profile All Condition aggravated Reports All Drugs Causing Condition aggravated AMISULPRIDE Demographics