Does PARATHYROID HORMONE Cause Product dose omission? 76 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 76 reports of Product dose omission have been filed in association with PARATHYROID HORMONE (NATPARA (parathyroid hormone)). This represents 1.7% of all adverse event reports for PARATHYROID HORMONE.
76
Reports of Product dose omission with PARATHYROID HORMONE
1.7%
of all PARATHYROID HORMONE reports
0
Deaths
37
Hospitalizations
How Dangerous Is Product dose omission From PARATHYROID HORMONE?
Of the 76 reports, 37 (48.7%) required hospitalization, and 11 (14.5%) were considered life-threatening.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PARATHYROID HORMONE. However, 76 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?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which PARATHYROID HORMONE Alternatives Have Lower Product dose omission Risk?
PARATHYROID HORMONE vs PARECOXIB
PARATHYROID HORMONE vs PARICALCITOL
PARATHYROID HORMONE vs PARITAPREVIR
PARATHYROID HORMONE vs PAROXETINE
PARATHYROID HORMONE vs PAROXETINE\PAROXETINE