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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 PEGINTRON Cause Incorrect product storage? 8 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Incorrect product storage have been filed in association with PEGINTRON. This represents 0.9% of all adverse event reports for PEGINTRON.

8
Reports of Incorrect product storage with PEGINTRON
0.9%
of all PEGINTRON reports
0
Deaths
1
Hospitalizations

How Dangerous Is Incorrect product storage From PEGINTRON?

Of the 8 reports, 1 (12.5%) required hospitalization.

Is Incorrect product storage Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for PEGINTRON. However, 8 reports have been filed with the FAERS database.

What Other Side Effects Does PEGINTRON Cause?

Anaemia (132) Fatigue (130) Product quality issue (118) Headache (96) Pyrexia (96) Nausea (93) Drug dose omission (85) No adverse event (77) Influenza like illness (75) White blood cell count decreased (74)

What Other Drugs Cause Incorrect product storage?

ETANERCEPT (2,149) INSULIN LISPRO (1,114) ABATACEPT (583) TERIPARATIDE (573) ADALIMUMAB (476) GOLIMUMAB (392) INSULIN GLARGINE (341) INSULIN HUMAN (336) USTEKINUMAB (299) ERYTHROPOIETIN (268)

Which PEGINTRON Alternatives Have Lower Incorrect product storage Risk?

PEGINTRON vs PEGLOTICASE PEGINTRON vs PEGUNIGALSIDASE ALFA-IWXJ PEGINTRON vs PEGVALIASE-PQPZ PEGINTRON vs PEGVISOMANT PEGINTRON vs PEGZEREPOETIN ALFA

Related Pages

PEGINTRON Full Profile All Incorrect product storage Reports All Drugs Causing Incorrect product storage PEGINTRON Demographics