Does PRAMLINTIDE Cause Device delivery system issue? 20 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 20 reports of Device delivery system issue have been filed in association with PRAMLINTIDE (SymlinPen). This represents 6.0% of all adverse event reports for PRAMLINTIDE.
20
Reports of Device delivery system issue with PRAMLINTIDE
6.0%
of all PRAMLINTIDE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Device delivery system issue From PRAMLINTIDE?
Of the 20 reports.
Is Device delivery system issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PRAMLINTIDE. However, 20 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 Device delivery system issue?
ALBUTEROL (9,509)
SOMATROPIN (1,848)
EXENATIDE (1,533)
BUDESONIDE\FORMOTEROL (1,260)
BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE (1,181)
BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM (523)
LEVALBUTEROL (459)
MOMETASONE FUROATE\OLOPATADINE (347)
ABATACEPT (342)
PEGFILGRASTIM (323)
Which PRAMLINTIDE Alternatives Have Lower Device delivery system issue Risk?
PRAMLINTIDE vs PRASTERONE
PRAMLINTIDE vs PRASUGREL
PRAMLINTIDE vs PRAVASTATIN
PRAMLINTIDE vs PRAVASTATIN\PRAVASTATIN
PRAMLINTIDE vs PRAZAXA