Does PARATHYROID HORMONE Cause Recalled product? 900 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 900 reports of Recalled product have been filed in association with PARATHYROID HORMONE (NATPARA (parathyroid hormone)). This represents 20.2% of all adverse event reports for PARATHYROID HORMONE.
900
Reports of Recalled product with PARATHYROID HORMONE
20.2%
of all PARATHYROID HORMONE reports
17
Deaths
389
Hospitalizations
How Dangerous Is Recalled product From PARATHYROID HORMONE?
Of the 900 reports, 17 (1.9%) resulted in death, 389 (43.2%) required hospitalization, and 437 (48.6%) 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 PARATHYROID HORMONE. However, 900 reports have been filed with the FAERS database.
What Other Side Effects Does PARATHYROID HORMONE Cause?
Hypocalcaemia (784)
Blood calcium decreased (703)
Paraesthesia (364)
Muscle spasms (357)
Headache (257)
Drug ineffective (217)
Blood calcium increased (212)
Nausea (201)
Inappropriate schedule of product administration (195)
Fatigue (191)
What Other Drugs Cause Recalled product?
ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT (80)
CALCITRIOL (68)
CALCIUM (66)
REMDESIVIR (36)
LEVOTHYROXINE\LIOTHYRONINE (34)
TESTOSTERONE (32)
VALSARTAN (32)
CHLORHEXIDINE (28)
ALCOHOL (26)
LEVOTHYROXINE (24)
Which PARATHYROID HORMONE Alternatives Have Lower Recalled product Risk?
PARATHYROID HORMONE vs PARECOXIB
PARATHYROID HORMONE vs PARICALCITOL
PARATHYROID HORMONE vs PARITAPREVIR
PARATHYROID HORMONE vs PAROXETINE
PARATHYROID HORMONE vs PAROXETINE\PAROXETINE