Does PRAMLINTIDE Cause Drug dose omission? 26 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 26 reports of Drug dose omission have been filed in association with PRAMLINTIDE (SymlinPen). This represents 7.8% of all adverse event reports for PRAMLINTIDE.
26
Reports of Drug dose omission with PRAMLINTIDE
7.8%
of all PRAMLINTIDE reports
0
Deaths
3
Hospitalizations
How Dangerous Is Drug dose omission From PRAMLINTIDE?
Of the 26 reports, 3 (11.5%) required hospitalization.
Is Drug dose omission 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)
Device issue (26)
Drug ineffective (26)
Device malfunction (25)
Incorrect dose administered by device (23)
Device delivery system issue (20)
What Other Drugs Cause Drug dose omission?
ETANERCEPT (10,871)
CINACALCET (8,683)
EVOLOCUMAB (4,914)
ADALIMUMAB (3,993)
INSULIN LISPRO (3,063)
GOLIMUMAB (2,652)
TERIPARATIDE (2,616)
APREMILAST (2,466)
ALBUTEROL (2,309)
FLUTICASONE\SALMETEROL (2,153)
Which PRAMLINTIDE Alternatives Have Lower Drug dose omission Risk?
PRAMLINTIDE vs PRASTERONE
PRAMLINTIDE vs PRASUGREL
PRAMLINTIDE vs PRAVASTATIN
PRAMLINTIDE vs PRAVASTATIN\PRAVASTATIN
PRAMLINTIDE vs PRAZAXA