Does REMIFENTANIL Cause Intentional product use issue? 18 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 18 reports of Intentional product use issue have been filed in association with REMIFENTANIL (Remifentanil Hydrochloride). This represents 0.7% of all adverse event reports for REMIFENTANIL.
18
Reports of Intentional product use issue with REMIFENTANIL
0.7%
of all REMIFENTANIL reports
4
Deaths
11
Hospitalizations
How Dangerous Is Intentional product use issue From REMIFENTANIL?
Of the 18 reports, 4 (22.2%) resulted in death, 11 (61.1%) required hospitalization, and 3 (16.7%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for REMIFENTANIL. However, 18 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 Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which REMIFENTANIL Alternatives Have Lower Intentional product use issue Risk?
REMIFENTANIL vs REMIMAZOLAM
REMIFENTANIL vs REMODULIN
REMIFENTANIL vs REPAGLINIDE
REMIFENTANIL vs REPOTRECTINIB
REMIFENTANIL vs REQUIP