Does PRAMLINTIDE Cause Incorrect dose administered by device? 23 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 23 reports of Incorrect dose administered by device have been filed in association with PRAMLINTIDE (SymlinPen). This represents 6.9% of all adverse event reports for PRAMLINTIDE.
23
Reports of Incorrect dose administered by device with PRAMLINTIDE
6.9%
of all PRAMLINTIDE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Incorrect dose administered by device From PRAMLINTIDE?
Of the 23 reports.
Is Incorrect dose administered by device Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PRAMLINTIDE. However, 23 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)
Device delivery system issue (20)
What Other Drugs Cause Incorrect dose administered by device?
EXENATIDE (3,332)
EVOLOCUMAB (2,840)
SOMATROPIN (2,486)
ALBUTEROL (1,236)
ETANERCEPT (1,032)
SECUKINUMAB (996)
ERENUMAB-AOOE (973)
BUDESONIDE\FORMOTEROL (753)
INSULIN GLARGINE (753)
BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE (674)
Which PRAMLINTIDE Alternatives Have Lower Incorrect dose administered by device Risk?
PRAMLINTIDE vs PRASTERONE
PRAMLINTIDE vs PRASUGREL
PRAMLINTIDE vs PRAVASTATIN
PRAMLINTIDE vs PRAVASTATIN\PRAVASTATIN
PRAMLINTIDE vs PRAZAXA