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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does PRAMLINTIDE Cause Adverse event? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Adverse event have been filed in association with PRAMLINTIDE (SymlinPen). This represents 1.5% of all adverse event reports for PRAMLINTIDE.

5
Reports of Adverse event with PRAMLINTIDE
1.5%
of all PRAMLINTIDE reports
0
Deaths
2
Hospitalizations

How Dangerous Is Adverse event From PRAMLINTIDE?

Of the 5 reports, 2 (40.0%) required hospitalization.

Is Adverse event Listed in the Official Label?

Yes, Adverse event is listed as a known adverse reaction in the official FDA drug label for PRAMLINTIDE.

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 Adverse event?

ABATACEPT (4,028) APIXABAN (3,871) ETANERCEPT (3,096) LENALIDOMIDE (2,426) INFLIXIMAB (2,269) ADALIMUMAB (2,121) METHOTREXATE (1,846) LEFLUNOMIDE (1,476) RIVAROXABAN (1,465) ALENDRONATE (1,462)

Which PRAMLINTIDE Alternatives Have Lower Adverse event Risk?

PRAMLINTIDE vs PRASTERONE PRAMLINTIDE vs PRASUGREL PRAMLINTIDE vs PRAVASTATIN PRAMLINTIDE vs PRAVASTATIN\PRAVASTATIN PRAMLINTIDE vs PRAZAXA

Related Pages

PRAMLINTIDE Full Profile All Adverse event Reports All Drugs Causing Adverse event PRAMLINTIDE Demographics