Does PRAMLINTIDE Cause Intentional product misuse? 31 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 31 reports of Intentional product misuse have been filed in association with PRAMLINTIDE (SymlinPen). This represents 9.3% of all adverse event reports for PRAMLINTIDE.
31
Reports of Intentional product misuse with PRAMLINTIDE
9.3%
of all PRAMLINTIDE reports
0
Deaths
2
Hospitalizations
How Dangerous Is Intentional product misuse From PRAMLINTIDE?
Of the 31 reports, 2 (6.5%) required hospitalization, and 1 (3.2%) were considered life-threatening.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PRAMLINTIDE. However, 31 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)
Device issue (26)
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 Intentional product misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
MINOXIDIL (2,418)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)
Which PRAMLINTIDE Alternatives Have Lower Intentional product misuse Risk?
PRAMLINTIDE vs PRASTERONE
PRAMLINTIDE vs PRASUGREL
PRAMLINTIDE vs PRAVASTATIN
PRAMLINTIDE vs PRAVASTATIN\PRAVASTATIN
PRAMLINTIDE vs PRAZAXA