Does PAROXETINE\PAROXETINE ANHYDROUS Cause Hypercalcaemia? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Hypercalcaemia have been filed in association with PAROXETINE\PAROXETINE ANHYDROUS. This represents 1.8% of all adverse event reports for PAROXETINE\PAROXETINE ANHYDROUS.
5
Reports of Hypercalcaemia with PAROXETINE\PAROXETINE ANHYDROUS
1.8%
of all PAROXETINE\PAROXETINE ANHYDROUS reports
0
Deaths
5
Hospitalizations
How Dangerous Is Hypercalcaemia From PAROXETINE\PAROXETINE ANHYDROUS?
Of the 5 reports, 5 (100.0%) required hospitalization.
Is Hypercalcaemia Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PAROXETINE\PAROXETINE ANHYDROUS. However, 5 reports have been filed with the FAERS database.
What Other Side Effects Does PAROXETINE\PAROXETINE ANHYDROUS Cause?
Drug-induced liver injury (36)
Off label use (33)
Drug ineffective (28)
Toxicity to various agents (24)
Insomnia (23)
Condition aggravated (22)
Product use in unapproved indication (22)
Paraesthesia (20)
Vomiting (20)
Abdominal discomfort (19)
What Other Drugs Cause Hypercalcaemia?
RITUXIMAB (857)
METHOTREXATE (803)
ADALIMUMAB (663)
TOCILIZUMAB (618)
ABATACEPT (612)
ETANERCEPT (602)
DENOSUMAB (599)
ALENDRONATE (594)
INFLIXIMAB (594)
LEFLUNOMIDE (585)
Which PAROXETINE\PAROXETINE ANHYDROUS Alternatives Have Lower Hypercalcaemia Risk?
PAROXETINE\PAROXETINE ANHYDROUS vs PASIREOTIDE
PAROXETINE\PAROXETINE ANHYDROUS vs PASIREOTIDE DIASPARTATE
PAROXETINE\PAROXETINE ANHYDROUS vs PATIROMER
PAROXETINE\PAROXETINE ANHYDROUS vs PATISIRAN
PAROXETINE\PAROXETINE ANHYDROUS vs PAXIL