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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 FOLATE Cause Condition aggravated? 28 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 28 reports of Condition aggravated have been filed in association with FOLATE (Foltira). This represents 3.0% of all adverse event reports for FOLATE.

28
Reports of Condition aggravated with FOLATE
3.0%
of all FOLATE reports
3
Deaths
27
Hospitalizations

How Dangerous Is Condition aggravated From FOLATE?

Of the 28 reports, 3 (10.7%) resulted in death, 27 (96.4%) required hospitalization.

Is Condition aggravated Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for FOLATE. However, 28 reports have been filed with the FAERS database.

What Other Side Effects Does FOLATE Cause?

Pneumonia (506) Asthma (495) Vomiting (487) Drug hypersensitivity (484) Oedema (473) Dyspnoea (448) Wheezing (435) Pain (270) Malaise (262) Respiratory tract infection (262)

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 FOLATE Alternatives Have Lower Condition aggravated Risk?

FOLATE vs FOLIC ACID FOLATE vs FOLINIC ACID FOLATE vs FOLLICLE STIMULATING HORMONE BETA POLYPEPTIDE\LUTROPIN ALFA FOLATE vs FOLLITROPIN FOLATE vs FOLLITROPIN ALFA

Related Pages

FOLATE Full Profile All Condition aggravated Reports All Drugs Causing Condition aggravated FOLATE Demographics