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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.

Recalled product: Which Medications Cause It? (1,687 Reports Across 49 Drugs)

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Recalled product has been reported as an adverse event with 49 different drugs in the FDA's FAERS database, with 1,687 total reports. 44 of these reports resulted in death.The drugs most commonly associated with Recalled product are PARATHYROID HORMONE, ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT, and CALCITRIOL.

1,687
Total Reports
49
Drugs Involved
44
Deaths
473
Hospitalizations
48.9 yrs
Average Patient Age
74.3% / 25.7%
Female / Male

Which Drugs Cause Recalled product Most Often?

Drug Reports % of Drug Reports Deaths Hosp. Life-Threat.
PARATHYROID HORMONE 900 20.2% 17 389 437
ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT 80 0.8% 0 5 1
CALCITRIOL 68 2.9% 2 38 12
CALCIUM 66 0.4% 2 36 13
REMDESIVIR 36 0.3% 8 3 0
LEVOTHYROXINE\LIOTHYRONINE 34 3.6% 0 4 4
TESTOSTERONE 32 0.1% 0 0 0
VALSARTAN 32 0.2% 1 7 5
CHLORHEXIDINE 28 0.3% 4 0 0
ALCOHOL 26 0.1% 0 1 0
LEVOTHYROXINE 24 0.0% 1 2 0
LOSARTAN 23 0.1% 2 5 5
HUMAN IMMUNOGLOBULIN G 22 0.0% 0 1 1
POTASSIUM 17 0.1% 5 3 0
ATROPINE\DIPHENOXYLATE 15 0.8% 1 2 0
HYDROCHLOROTHIAZIDE\VALSARTAN 14 0.2% 0 4 4
LANSOPRAZOLE 14 0.0% 0 1 0
METFORMIN 14 0.0% 0 0 0
ARIPIPRAZOLE 13 0.0% 0 2 0
GUANFACINE 13 0.4% 0 1 2

View all 49 drugs →

Top 3 Drugs Associated With Recalled product

900 reports
68 reports

Related Side Effects

Drug ineffective (1,049,718) Off label use (762,782) Death (660,423) Fatigue (599,248) Nausea (562,301) Diarrhoea (491,550) Pain (471,975) Headache (460,069) Dyspnoea (409,496) Dizziness (352,922)