Does PRAMLINTIDE Cause Product quality issue? 16 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Product quality issue have been filed in association with PRAMLINTIDE (SymlinPen). This represents 4.8% of all adverse event reports for PRAMLINTIDE.
16
Reports of Product quality issue with PRAMLINTIDE
4.8%
of all PRAMLINTIDE reports
0
Deaths
2
Hospitalizations
How Dangerous Is Product quality issue From PRAMLINTIDE?
Of the 16 reports, 2 (12.5%) 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 PRAMLINTIDE. However, 16 reports have been filed with the FAERS database.
What Other Side Effects Does PRAMLINTIDE Cause?
Blood glucose increased (106)
Nausea (59)
Weight decreased (36)
Blood glucose decreased (35)
Intentional product misuse (31)
Device issue (26)
Drug dose omission (26)
Drug ineffective (26)
Device malfunction (25)
Incorrect dose administered by device (23)
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 PRAMLINTIDE Alternatives Have Lower Product quality issue Risk?
PRAMLINTIDE vs PRASTERONE
PRAMLINTIDE vs PRASUGREL
PRAMLINTIDE vs PRAVASTATIN
PRAMLINTIDE vs PRAVASTATIN\PRAVASTATIN
PRAMLINTIDE vs PRAZAXA