Does PRAMLINTIDE Cause Wrong technique in device usage process? 16 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Wrong technique in device usage process have been filed in association with PRAMLINTIDE (SymlinPen). This represents 4.8% of all adverse event reports for PRAMLINTIDE.
16
Reports of Wrong technique in device usage process with PRAMLINTIDE
4.8%
of all PRAMLINTIDE reports
0
Deaths
1
Hospitalizations
How Dangerous Is Wrong technique in device usage process From PRAMLINTIDE?
Of the 16 reports, 1 (6.3%) required hospitalization.
Is Wrong technique in device usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PRAMLINTIDE. However, 16 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 Wrong technique in device usage process?
ALBUTEROL (5,380)
SOMATROPIN (4,746)
EXENATIDE (3,255)
FLUTICASONE FUROATE\UMECLIDINIUM\VILANTEROL TRIFENATATE (2,673)
FLUTICASONE\SALMETEROL (2,259)
FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (2,197)
INSULIN GLARGINE (1,749)
UMECLIDINIUM\VILANTEROL TRIFENATATE (1,531)
BUDESONIDE\FORMOTEROL (1,481)
BELIMUMAB (1,347)
Which PRAMLINTIDE Alternatives Have Lower Wrong technique in device usage process Risk?
PRAMLINTIDE vs PRASTERONE
PRAMLINTIDE vs PRASUGREL
PRAMLINTIDE vs PRAVASTATIN
PRAMLINTIDE vs PRAVASTATIN\PRAVASTATIN
PRAMLINTIDE vs PRAZAXA