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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 TRIMETHOPRIM Cause Haemoglobin decreased? 60 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 60 reports of Haemoglobin decreased have been filed in association with TRIMETHOPRIM (Trimethoprim). This represents 1.9% of all adverse event reports for TRIMETHOPRIM.

60
Reports of Haemoglobin decreased with TRIMETHOPRIM
1.9%
of all TRIMETHOPRIM reports
14
Deaths
32
Hospitalizations

How Dangerous Is Haemoglobin decreased From TRIMETHOPRIM?

Of the 60 reports, 14 (23.3%) resulted in death, 32 (53.3%) required hospitalization, and 15 (25.0%) were considered life-threatening.

Is Haemoglobin decreased Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TRIMETHOPRIM. However, 60 reports have been filed with the FAERS database.

What Other Side Effects Does TRIMETHOPRIM Cause?

Headache (409) Nausea (383) Off label use (376) Drug ineffective (368) Malaise (346) Swelling face (267) Hypersensitivity (260) Acute kidney injury (249) Rash (235) Drug intolerance (231)

What Other Drugs Cause Haemoglobin decreased?

LENALIDOMIDE (4,031) RUXOLITINIB (3,297) ECULIZUMAB (3,028) ADALIMUMAB (2,459) CLOZAPINE (2,396) RITUXIMAB (1,803) APIXABAN (1,779) NIRAPARIB (1,759) METHOTREXATE (1,754) RIBAVIRIN (1,753)

Which TRIMETHOPRIM Alternatives Have Lower Haemoglobin decreased Risk?

TRIMETHOPRIM vs TRIMIPRAMINE TRIMETHOPRIM vs TRIPROLIDINE TRIMETHOPRIM vs TRIPTORELIN TRIMETHOPRIM vs TRISODIUM TRIMETHOPRIM vs TROFINETIDE

Related Pages

TRIMETHOPRIM Full Profile All Haemoglobin decreased Reports All Drugs Causing Haemoglobin decreased TRIMETHOPRIM Demographics