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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does CALCIUM\VITAMIN D Cause Condition aggravated? 101 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 101 reports of Condition aggravated have been filed in association with CALCIUM\VITAMIN D. This represents 21.3% of all adverse event reports for CALCIUM\VITAMIN D.

101
Reports of Condition aggravated with CALCIUM\VITAMIN D
21.3%
of all CALCIUM\VITAMIN D reports
58
Deaths
75
Hospitalizations

How Dangerous Is Condition aggravated From CALCIUM\VITAMIN D?

Of the 101 reports, 58 (57.4%) resulted in death, 75 (74.3%) required hospitalization, and 60 (59.4%) were considered life-threatening.

Is Condition aggravated Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for CALCIUM\VITAMIN D. However, 101 reports have been filed with the FAERS database.

What Other Side Effects Does CALCIUM\VITAMIN D Cause?

Nausea (115) Drug ineffective (108) Off label use (104) Dyspnoea (97) Constipation (90) Therapeutic product effect incomplete (89) Pain (87) Abdominal pain (86) Headache (86) Dyspepsia (80)

What Other Drugs Cause Condition aggravated?

TOFACITINIB (16,925) INFLIXIMAB (16,616) DUPILUMAB (16,459) ETANERCEPT (15,897) METHOTREXATE (14,938) ADALIMUMAB (13,527) PREDNISONE (10,751) INFLIXIMAB-DYYB (10,275) HYDROXYCHLOROQUINE (8,848) RITUXIMAB (8,627)

Which CALCIUM\VITAMIN D Alternatives Have Lower Condition aggravated Risk?

CALCIUM\VITAMIN D vs CAMPHOR \MENTHOL CALCIUM\VITAMIN D vs CAMRELIZUMAB CALCIUM\VITAMIN D vs CANAGLIFLOZIN CALCIUM\VITAMIN D vs CANAGLIFLOZIN\METFORMIN CALCIUM\VITAMIN D vs CANAKINUMAB

Related Pages

CALCIUM\VITAMIN D Full Profile All Condition aggravated Reports All Drugs Causing Condition aggravated CALCIUM\VITAMIN D Demographics