Does DUROGESIC DTRANS 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 DUROGESIC DTRANS. This represents 18.0% of all adverse event reports for DUROGESIC DTRANS.
7
Reports of Product quality issue with DUROGESIC DTRANS
18.0%
of all DUROGESIC DTRANS reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product quality issue From DUROGESIC DTRANS?
Of the 7 reports.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DUROGESIC DTRANS. However, 7 reports have been filed with the FAERS database.
What Other Side Effects Does DUROGESIC DTRANS Cause?
Wrong technique in drug usage process (22)
Product adhesion issue (12)
Drug abuse (6)
Inappropriate schedule of drug administration (6)
Drug ineffective (5)
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)