Does SEVOFLURANE Cause Product quality issue? 30 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 30 reports of Product quality issue have been filed in association with SEVOFLURANE (Sojourn). This represents 0.7% of all adverse event reports for SEVOFLURANE.
30
Reports of Product quality issue with SEVOFLURANE
0.7%
of all SEVOFLURANE reports
0
Deaths
3
Hospitalizations
How Dangerous Is Product quality issue From SEVOFLURANE?
Of the 30 reports, 3 (10.0%) required hospitalization, and 2 (6.7%) were considered life-threatening.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SEVOFLURANE. However, 30 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 quality issue?
ETONOGESTREL (4,651)
ALBUTEROL (4,466)
TIOTROPIUM (3,821)
MOMETASONE FUROATE (3,406)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
EXENATIDE (1,839)
Which SEVOFLURANE Alternatives Have Lower Product quality issue Risk?
SEVOFLURANE vs SEVOFLURANE, USP
SEVOFLURANE vs SIBUTRAMINE
SEVOFLURANE vs SILDENAFIL
SEVOFLURANE vs SILODOSIN
SEVOFLURANE vs SILTUXIMAB