Does PARATHYROID HORMONE Cause Product dose omission issue? 165 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 165 reports of Product dose omission issue have been filed in association with PARATHYROID HORMONE (NATPARA (parathyroid hormone)). This represents 3.7% of all adverse event reports for PARATHYROID HORMONE.
165
Reports of Product dose omission issue with PARATHYROID HORMONE
3.7%
of all PARATHYROID HORMONE reports
8
Deaths
91
Hospitalizations
How Dangerous Is Product dose omission issue From PARATHYROID HORMONE?
Of the 165 reports, 8 (4.8%) resulted in death, 91 (55.2%) required hospitalization, and 24 (14.5%) were considered life-threatening.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PARATHYROID HORMONE. However, 165 reports have been filed with the FAERS database.
What Other Side Effects Does PARATHYROID HORMONE Cause?
Recalled product (900)
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)
What Other Drugs Cause Product dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which PARATHYROID HORMONE Alternatives Have Lower Product dose omission issue Risk?
PARATHYROID HORMONE vs PARECOXIB
PARATHYROID HORMONE vs PARICALCITOL
PARATHYROID HORMONE vs PARITAPREVIR
PARATHYROID HORMONE vs PAROXETINE
PARATHYROID HORMONE vs PAROXETINE\PAROXETINE