Does SANDOZ FENTANYL SYSTEM Cause Product quality issue? 69 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 69 reports of Product quality issue have been filed in association with SANDOZ FENTANYL SYSTEM. This represents 61.1% of all adverse event reports for SANDOZ FENTANYL SYSTEM.
69
Reports of Product quality issue with SANDOZ FENTANYL SYSTEM
61.1%
of all SANDOZ FENTANYL SYSTEM reports
0
Deaths
8
Hospitalizations
How Dangerous Is Product quality issue From SANDOZ FENTANYL SYSTEM?
Of the 69 reports, 8 (11.6%) 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 SANDOZ FENTANYL SYSTEM. However, 69 reports have been filed with the FAERS database.
What Other Side Effects Does SANDOZ FENTANYL SYSTEM Cause?
Wrong technique in drug usage process (71)
Drug ineffective (41)
Product adhesion issue (30)
Pain (19)
Drug dose omission (14)
Inappropriate schedule of drug administration (12)
Poor quality drug administered (12)
Drug effect decreased (11)
Drug administered at inappropriate site (10)
Therapeutic response decreased (9)
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 SANDOZ FENTANYL SYSTEM Alternatives Have Lower Product quality issue Risk?
SANDOZ FENTANYL SYSTEM vs SAPROPTERIN
SANDOZ FENTANYL SYSTEM vs SAQUINAVIR
SANDOZ FENTANYL SYSTEM vs SARECYCLINE
SANDOZ FENTANYL SYSTEM vs SARGRAMOSTIM
SANDOZ FENTANYL SYSTEM vs SARILUMAB