Does FENTANYL SYSTEM Cause Product quality issue? 18 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 18 reports of Product quality issue have been filed in association with FENTANYL SYSTEM. This represents 4.1% of all adverse event reports for FENTANYL SYSTEM.
18
Reports of Product quality issue with FENTANYL SYSTEM
4.1%
of all FENTANYL SYSTEM reports
0
Deaths
3
Hospitalizations
How Dangerous Is Product quality issue From FENTANYL SYSTEM?
Of the 18 reports, 3 (16.7%) 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 FENTANYL SYSTEM. However, 18 reports have been filed with the FAERS database.
What Other Side Effects Does FENTANYL SYSTEM Cause?
Pain (79)
Wrong technique in drug usage process (62)
Drug effect decreased (60)
Drug ineffective (58)
Drug withdrawal syndrome (40)
Toxicity to various agents (39)
Intentional drug misuse (35)
Drug abuse (31)
Hyperhidrosis (31)
Application site pruritus (28)
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 FENTANYL SYSTEM Alternatives Have Lower Product quality issue Risk?
FENTANYL SYSTEM vs FENTANYL\FENTANYL
FENTANYL SYSTEM vs FENTORA
FENTANYL SYSTEM vs FERRIC ANHYDROUS
FENTANYL SYSTEM vs FERRIC CARBOXYMALTOSE
FENTANYL SYSTEM vs FERRIC DERISOMALTOSE