Does UNSPECIFIED FENTANYL SYSTEM Cause Product quality issue? 13 Reports in FDA Database
Grow Your Own Natural Pharmacy at Home
Medicinal Garden Kit — 10 healing herbs, 4,818 seeds + step-by-step guide.
According to the FDA Adverse Event Reporting System (FAERS), 13 reports of Product quality issue have been filed in association with UNSPECIFIED FENTANYL SYSTEM. This represents 81.3% of all adverse event reports for UNSPECIFIED FENTANYL SYSTEM.
13
Reports of Product quality issue with UNSPECIFIED FENTANYL SYSTEM
81.3%
of all UNSPECIFIED FENTANYL SYSTEM reports
1
Deaths
3
Hospitalizations
How Dangerous Is Product quality issue From UNSPECIFIED FENTANYL SYSTEM?
Of the 13 reports, 1 (7.7%) resulted in death, 3 (23.1%) 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 SYSTEM. However, 13 reports have been filed with the FAERS database.
What Other Side Effects Does UNSPECIFIED FENTANYL SYSTEM 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)