Does PRAMLINTIDE Cause Device issue? 26 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 26 reports of Device issue have been filed in association with PRAMLINTIDE (SymlinPen). This represents 7.8% of all adverse event reports for PRAMLINTIDE.
26
Reports of Device issue with PRAMLINTIDE
7.8%
of all PRAMLINTIDE reports
0
Deaths
1
Hospitalizations
How Dangerous Is Device issue From PRAMLINTIDE?
Of the 26 reports, 1 (3.8%) required hospitalization, and 1 (3.8%) were considered life-threatening.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PRAMLINTIDE. However, 26 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)
Drug dose omission (26)
Drug ineffective (26)
Device malfunction (25)
Incorrect dose administered by device (23)
Device delivery system issue (20)
What Other Drugs Cause Device issue?
ADALIMUMAB (17,630)
SOMATROPIN (5,131)
PEGFILGRASTIM (5,071)
ETANERCEPT (4,143)
INSULIN GLARGINE (3,175)
EXENATIDE (2,862)
LEVONORGESTREL (2,623)
CARBIDOPA\LEVODOPA (2,574)
GOLIMUMAB (1,827)
USTEKINUMAB (1,716)
Which PRAMLINTIDE Alternatives Have Lower Device issue Risk?
PRAMLINTIDE vs PRASTERONE
PRAMLINTIDE vs PRASUGREL
PRAMLINTIDE vs PRAVASTATIN
PRAMLINTIDE vs PRAVASTATIN\PRAVASTATIN
PRAMLINTIDE vs PRAZAXA