Does SEVOFLURANE Cause Product use issue? 24 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 24 reports of Product use issue have been filed in association with SEVOFLURANE (Sojourn). This represents 0.6% of all adverse event reports for SEVOFLURANE.
24
Reports of Product use issue with SEVOFLURANE
0.6%
of all SEVOFLURANE reports
1
Deaths
12
Hospitalizations
How Dangerous Is Product use issue From SEVOFLURANE?
Of the 24 reports, 1 (4.2%) resulted in death, 12 (50.0%) required hospitalization, and 4 (16.7%) 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 SEVOFLURANE. However, 24 reports have been filed with the FAERS database.
What Other Side Effects Does SEVOFLURANE Cause?
Hypotension (316)
Anaesthetic complication neurological (260)
Acute kidney injury (212)
Hyperthermia malignant (207)
Cardiac arrest (159)
Tachycardia (159)
Bradycardia (155)
Drug ineffective (147)
Oxygen saturation decreased (129)
Post procedural complication (129)
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 SEVOFLURANE Alternatives Have Lower Product use issue Risk?
SEVOFLURANE vs SEVOFLURANE, USP
SEVOFLURANE vs SIBUTRAMINE
SEVOFLURANE vs SILDENAFIL
SEVOFLURANE vs SILODOSIN
SEVOFLURANE vs SILTUXIMAB