CALCIUM ACETATE

Generic: CALCIUM ACETATE

Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.Manufacturer
ORALRoute
CALCIUM ACETATEActive Substance
2015-06-29Original Approval

CALCIUM ACETATE is FDA application ANDA202315, sponsored by HERITAGE PHARMS INC. Any recalls listed below come from FDA drug enforcement reports, and reaction counts are the number of FAERS adverse event reports that mention the drug and that reaction; a report does not prove the drug caused it.

Recalls

Class II2021-03-15
Calcium Acetate Capsules 667 mg 200 Capsules Rx only NDC 23155-531-02 Manufactured for: Heritage Pharmaceuticals Inc. Ea

CGMP Deviations: Intermittent exposure to temperature excursion during storage.

Top Reported Reactions

1
RENAL FAILURE
484 reports
2
CHRONIC KIDNEY DISEASE
464 reports
3
END STAGE RENAL DISEASE
436 reports
4
ACUTE KIDNEY INJURY
378 reports
5
DIARRHOEA
333 reports
6
NAUSEA
268 reports
7
FATIGUE
255 reports
8
DEATH
243 reports
9
DYSPNOEA
231 reports
10
NEPHROGENIC ANAEMIA
213 reports