Does REMIFENTANIL Cause Product use issue? 9 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Product use issue have been filed in association with REMIFENTANIL (Remifentanil Hydrochloride). This represents 0.3% of all adverse event reports for REMIFENTANIL.
9
Reports of Product use issue with REMIFENTANIL
0.3%
of all REMIFENTANIL reports
0
Deaths
4
Hospitalizations
How Dangerous Is Product use issue From REMIFENTANIL?
Of the 9 reports, 4 (44.4%) required hospitalization, and 1 (11.1%) were considered life-threatening.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for REMIFENTANIL. However, 9 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 use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which REMIFENTANIL Alternatives Have Lower Product use issue Risk?
REMIFENTANIL vs REMIMAZOLAM
REMIFENTANIL vs REMODULIN
REMIFENTANIL vs REPAGLINIDE
REMIFENTANIL vs REPOTRECTINIB
REMIFENTANIL vs REQUIP