Does PARATHYROID HORMONE Cause Device defective? 22 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 22 reports of Device defective have been filed in association with PARATHYROID HORMONE (NATPARA (parathyroid hormone)). This represents 0.5% of all adverse event reports for PARATHYROID HORMONE.
22
Reports of Device defective with PARATHYROID HORMONE
0.5%
of all PARATHYROID HORMONE reports
0
Deaths
12
Hospitalizations
How Dangerous Is Device defective From PARATHYROID HORMONE?
Of the 22 reports, 12 (54.5%) required hospitalization, and 2 (9.1%) were considered life-threatening.
Is Device defective Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PARATHYROID HORMONE. However, 22 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 Device defective?
SOMATROPIN (1,719)
USTEKINUMAB (1,071)
SECUKINUMAB (666)
GUSELKUMAB (574)
GOLIMUMAB (539)
ABATACEPT (458)
ALBUTEROL (445)
TOCILIZUMAB (400)
INSULIN GLARGINE (397)
EXENATIDE (387)
Which PARATHYROID HORMONE Alternatives Have Lower Device defective Risk?
PARATHYROID HORMONE vs PARECOXIB
PARATHYROID HORMONE vs PARICALCITOL
PARATHYROID HORMONE vs PARITAPREVIR
PARATHYROID HORMONE vs PAROXETINE
PARATHYROID HORMONE vs PAROXETINE\PAROXETINE