Does PRAMLINTIDE Cause Device malfunction? 25 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 25 reports of Device malfunction have been filed in association with PRAMLINTIDE (SymlinPen). This represents 7.5% of all adverse event reports for PRAMLINTIDE.
25
Reports of Device malfunction with PRAMLINTIDE
7.5%
of all PRAMLINTIDE reports
0
Deaths
3
Hospitalizations
How Dangerous Is Device malfunction From PRAMLINTIDE?
Of the 25 reports, 3 (12.0%) required hospitalization.
Is Device malfunction Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PRAMLINTIDE. However, 25 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)
Incorrect dose administered by device (23)
Device delivery system issue (20)
What Other Drugs Cause Device malfunction?
PEGFILGRASTIM (6,818)
EXENATIDE (3,273)
BUDESONIDE\FORMOTEROL (2,771)
ABATACEPT (2,459)
SOMATROPIN (2,311)
GOLIMUMAB (2,293)
SECUKINUMAB (2,259)
ALBUTEROL (2,257)
GUSELKUMAB (1,410)
MOMETASONE FUROATE (1,332)
Which PRAMLINTIDE Alternatives Have Lower Device malfunction Risk?
PRAMLINTIDE vs PRASTERONE
PRAMLINTIDE vs PRASUGREL
PRAMLINTIDE vs PRAVASTATIN
PRAMLINTIDE vs PRAVASTATIN\PRAVASTATIN
PRAMLINTIDE vs PRAZAXA