Does FOLATE Cause Intentional product use issue? 40 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 40 reports of Intentional product use issue have been filed in association with FOLATE (Foltira). This represents 4.3% of all adverse event reports for FOLATE.
40
Reports of Intentional product use issue with FOLATE
4.3%
of all FOLATE reports
29
Deaths
34
Hospitalizations
How Dangerous Is Intentional product use issue From FOLATE?
Of the 40 reports, 29 (72.5%) resulted in death, 34 (85.0%) required hospitalization, and 2 (5.0%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FOLATE. However, 40 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 Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which FOLATE Alternatives Have Lower Intentional product use issue 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