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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 REMIFENTANIL Cause Product administration error? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Product administration error have been filed in association with REMIFENTANIL (Remifentanil Hydrochloride). This represents 0.2% of all adverse event reports for REMIFENTANIL.

5
Reports of Product administration error with REMIFENTANIL
0.2%
of all REMIFENTANIL reports
2
Deaths
0
Hospitalizations

How Dangerous Is Product administration error From REMIFENTANIL?

Of the 5 reports, 2 (40.0%) resulted in death.

Is Product administration error Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for REMIFENTANIL. However, 5 reports have been filed with the FAERS database.

What Other Side Effects Does REMIFENTANIL Cause?

Anaphylactic shock (351) Hypotension (195) Anaphylactic reaction (178) Cardiac arrest (145) Bradycardia (132) Foetal exposure during pregnancy (132) Drug ineffective (112) Off label use (109) Anaesthetic complication neurological (96) Premature baby (91)

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 REMIFENTANIL Alternatives Have Lower Product administration error Risk?

REMIFENTANIL vs REMIMAZOLAM REMIFENTANIL vs REMODULIN REMIFENTANIL vs REPAGLINIDE REMIFENTANIL vs REPOTRECTINIB REMIFENTANIL vs REQUIP

Related Pages

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