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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 RISDIPLAM Cause Product administration error? 9 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Product administration error have been filed in association with RISDIPLAM (EVRYSDI). This represents 0.3% of all adverse event reports for RISDIPLAM.

9
Reports of Product administration error with RISDIPLAM
0.3%
of all RISDIPLAM reports
0
Deaths
2
Hospitalizations

How Dangerous Is Product administration error From RISDIPLAM?

Of the 9 reports, 2 (22.2%) required hospitalization.

Is Product administration error Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for RISDIPLAM. However, 9 reports have been filed with the FAERS database.

What Other Side Effects Does RISDIPLAM Cause?

No adverse event (324) Diarrhoea (280) Asthenia (209) Pneumonia (182) Death (165) Pyrexia (152) Fatigue (145) Muscular weakness (125) Vomiting (121) Drug ineffective (115)

What Other Drugs Cause Product administration error?

HYDROXYPROGESTERONE CAPROATE (972) ACETAMINOPHEN (666) CENEGERMIN-BKBJ (613) LEUPROLIDE (595) EVOLOCUMAB (565) ADALIMUMAB (543) METHYLPHENIDATE (414) OLMESARTAN MEDOXOMIL (314) ASPIRIN (241) SECUKINUMAB (225)

Which RISDIPLAM Alternatives Have Lower Product administration error Risk?

RISDIPLAM vs RISEDRONATE RISDIPLAM vs RISEDRONIC ACID RISDIPLAM vs RISPERDAL RISDIPLAM vs RISPERDAL CONSTA RISDIPLAM vs RISPERIDONE

Related Pages

RISDIPLAM Full Profile All Product administration error Reports All Drugs Causing Product administration error RISDIPLAM Demographics