Does UNSPECIFIED FENTANYL Cause Product quality issue? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Product quality issue have been filed in association with UNSPECIFIED FENTANYL. This represents 58.3% of all adverse event reports for UNSPECIFIED FENTANYL.
7
Reports of Product quality issue with UNSPECIFIED FENTANYL
58.3%
of all UNSPECIFIED FENTANYL reports
0
Deaths
4
Hospitalizations
How Dangerous Is Product quality issue From UNSPECIFIED FENTANYL?
Of the 7 reports, 4 (57.1%) required hospitalization.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for UNSPECIFIED FENTANYL. However, 7 reports have been filed with the FAERS database.
What Other Side Effects Does UNSPECIFIED FENTANYL Cause?
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)