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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 TRASTUZUMAB-DTTB Cause Condition aggravated? 19 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 19 reports of Condition aggravated have been filed in association with TRASTUZUMAB-DTTB. This represents 3.8% of all adverse event reports for TRASTUZUMAB-DTTB.

19
Reports of Condition aggravated with TRASTUZUMAB-DTTB
3.8%
of all TRASTUZUMAB-DTTB reports
0
Deaths
13
Hospitalizations

How Dangerous Is Condition aggravated From TRASTUZUMAB-DTTB?

Of the 19 reports, 13 (68.4%) required hospitalization.

Is Condition aggravated Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TRASTUZUMAB-DTTB. However, 19 reports have been filed with the FAERS database.

What Other Side Effects Does TRASTUZUMAB-DTTB Cause?

Diarrhoea (150) Product use in unapproved indication (89) Nausea (66) Pyrexia (65) Off label use (63) Anaemia (61) Vomiting (46) Hypokalaemia (43) Chills (40) Dyspnoea (37)

What Other Drugs Cause Condition aggravated?

TOFACITINIB (16,925) INFLIXIMAB (16,616) DUPILUMAB (16,459) ETANERCEPT (15,897) METHOTREXATE (14,938) ADALIMUMAB (13,527) PREDNISONE (10,751) INFLIXIMAB-DYYB (10,275) HYDROXYCHLOROQUINE (8,848) RITUXIMAB (8,627)

Which TRASTUZUMAB-DTTB Alternatives Have Lower Condition aggravated Risk?

TRASTUZUMAB-DTTB vs TRASTUZUMAB EMTANSINE TRASTUZUMAB-DTTB vs TRASTUZUMAB-PKRB TRASTUZUMAB-DTTB vs TRASTUZUMAB-QYYP TRASTUZUMAB-DTTB vs TRAVOPROST TRASTUZUMAB-DTTB vs TRAZODONE

Related Pages

TRASTUZUMAB-DTTB Full Profile All Condition aggravated Reports All Drugs Causing Condition aggravated TRASTUZUMAB-DTTB Demographics