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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 PANITUMUMAB Cause Therapy partial responder? 402 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 402 reports of Therapy partial responder have been filed in association with PANITUMUMAB (Vectibix). This represents 3.7% of all adverse event reports for PANITUMUMAB.

402
Reports of Therapy partial responder with PANITUMUMAB
3.7%
of all PANITUMUMAB reports
103
Deaths
37
Hospitalizations

How Dangerous Is Therapy partial responder From PANITUMUMAB?

Of the 402 reports, 103 (25.6%) resulted in death, 37 (9.2%) required hospitalization, and 38 (9.5%) were considered life-threatening.

Is Therapy partial responder Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for PANITUMUMAB. However, 402 reports have been filed with the FAERS database.

What Other Side Effects Does PANITUMUMAB Cause?

Rash (1,392) Diarrhoea (1,123) Death (767) Dermatitis acneiform (758) Neutropenia (757) Skin toxicity (728) Neuropathy peripheral (613) Hypomagnesaemia (611) Nausea (608) Disease progression (600)

What Other Drugs Cause Therapy partial responder?

CYCLOPHOSPHAMIDE (1,397) RITUXIMAB (1,219) DEXAMETHASONE (1,199) PREDNISONE (1,176) PEMBROLIZUMAB (1,125) CARBOPLATIN (1,096) DOXORUBICIN (834) METHOTREXATE (775) VINCRISTINE (707) ETOPOSIDE (670)

Which PANITUMUMAB Alternatives Have Lower Therapy partial responder Risk?

PANITUMUMAB vs PANOBINOSTAT PANITUMUMAB vs PANTOPRAZOLE PANITUMUMAB vs PANTOPRAZOLE ANHYDROUS PANITUMUMAB vs PANTOTHENIC ACID PANITUMUMAB vs PAPAVERINE

Related Pages

PANITUMUMAB Full Profile All Therapy partial responder Reports All Drugs Causing Therapy partial responder PANITUMUMAB Demographics