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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 INVESTIGATIONAL PRODUCT Cause Incorrect dose administered? 7 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Incorrect dose administered have been filed in association with INVESTIGATIONAL PRODUCT. This represents 0.1% of all adverse event reports for INVESTIGATIONAL PRODUCT.

7
Reports of Incorrect dose administered with INVESTIGATIONAL PRODUCT
0.1%
of all INVESTIGATIONAL PRODUCT reports
0
Deaths
2
Hospitalizations

How Dangerous Is Incorrect dose administered From INVESTIGATIONAL PRODUCT?

Of the 7 reports, 2 (28.6%) required hospitalization.

Is Incorrect dose administered Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for INVESTIGATIONAL PRODUCT. However, 7 reports have been filed with the FAERS database.

What Other Side Effects Does INVESTIGATIONAL PRODUCT Cause?

Febrile neutropenia (241) Pneumonia (229) Acute kidney injury (198) Pyrexia (189) Anaemia (176) Diarrhoea (170) Sepsis (168) Dyspnoea (156) Nausea (134) Hypotension (130)

What Other Drugs Cause Incorrect dose administered?

TIRZEPATIDE (23,301) ADALIMUMAB (14,000) DUPILUMAB (9,907) RANITIDINE (9,337) INSULIN LISPRO (8,318) ACETAMINOPHEN (5,316) DULAGLUTIDE (5,207) SECUKINUMAB (4,524) INSULIN GLARGINE (3,070) SOMATROPIN (2,772)

Which INVESTIGATIONAL PRODUCT Alternatives Have Lower Incorrect dose administered Risk?

INVESTIGATIONAL PRODUCT vs INVOKANA INVESTIGATIONAL PRODUCT vs IOBENGUANE I-131 INVESTIGATIONAL PRODUCT vs IOBITRIDOL INVESTIGATIONAL PRODUCT vs IODINE INVESTIGATIONAL PRODUCT vs IODINE\IOFLUPANE I-123

Related Pages

INVESTIGATIONAL PRODUCT Full Profile All Incorrect dose administered Reports All Drugs Causing Incorrect dose administered INVESTIGATIONAL PRODUCT Demographics