Does HOMEOPATHICS Cause Recalled product? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Recalled product have been filed in association with HOMEOPATHICS. This represents 0.6% of all adverse event reports for HOMEOPATHICS.
6
Reports of Recalled product with HOMEOPATHICS
0.6%
of all HOMEOPATHICS reports
0
Deaths
1
Hospitalizations
How Dangerous Is Recalled product From HOMEOPATHICS?
Of the 6 reports, 1 (16.7%) required hospitalization, and 2 (33.3%) were considered life-threatening.
Is Recalled product Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for HOMEOPATHICS. However, 6 reports have been filed with the FAERS database.
What Other Side Effects Does HOMEOPATHICS Cause?
Seizure (229)
Anosmia (86)
Drug ineffective (70)
Ageusia (66)
Vomiting (58)
Dyspnoea (53)
Rash (45)
Hypersensitivity (36)
Pyrexia (35)
Product use issue (34)
What Other Drugs Cause Recalled product?
PARATHYROID HORMONE (900)
ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT (80)
CALCITRIOL (68)
CALCIUM (66)
REMDESIVIR (36)
LEVOTHYROXINE\LIOTHYRONINE (34)
TESTOSTERONE (32)
VALSARTAN (32)
CHLORHEXIDINE (28)
ALCOHOL (26)
Which HOMEOPATHICS Alternatives Have Lower Recalled product Risk?
HOMEOPATHICS vs HOMEOPATHICS\ZINC\ZINC
HOMEOPATHICS vs HORSE CHESTNUT
HOMEOPATHICS vs HUMALOG
HOMEOPATHICS vs HUMALOG LISPRO
HOMEOPATHICS vs HUMALOG LISPRO, NPL