Does FOLIC ACID Cause Incorrect product administration duration? 70 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 70 reports of Incorrect product administration duration have been filed in association with FOLIC ACID (Folic Acid). This represents 0.3% of all adverse event reports for FOLIC ACID.
70
Reports of Incorrect product administration duration with FOLIC ACID
0.3%
of all FOLIC ACID reports
59
Deaths
65
Hospitalizations
How Dangerous Is Incorrect product administration duration From FOLIC ACID?
Of the 70 reports, 59 (84.3%) resulted in death, 65 (92.9%) required hospitalization, and 58 (82.9%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FOLIC ACID. However, 70 reports have been filed with the FAERS database.
What Other Side Effects Does FOLIC ACID Cause?
Pain (8,813)
Drug ineffective (8,375)
Systemic lupus erythematosus (8,360)
Alopecia (8,294)
Pemphigus (8,128)
Rheumatoid arthritis (8,125)
Abdominal discomfort (8,084)
Fatigue (7,888)
Glossodynia (7,433)
Swelling (6,599)
What Other Drugs Cause Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which FOLIC ACID Alternatives Have Lower Incorrect product administration duration Risk?
FOLIC ACID vs FOLINIC ACID
FOLIC ACID vs FOLLICLE STIMULATING HORMONE BETA POLYPEPTIDE\LUTROPIN ALFA
FOLIC ACID vs FOLLITROPIN
FOLIC ACID vs FOLLITROPIN ALFA
FOLIC ACID vs FOLLITROPIN BETA