The Safety Rates Drug Report

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Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
127216061 12721606 1 I 20160823 20160907 20160907 EXP US-IPCA LABORATORIES LIMITED-IPC201609-000753 IPCA BAZARI H,PALMER W,BARON J,ARMSTRONG K. CASE 24-2016: A 66-YEAR-OLD MAN WITH MALAISE, WEAKNESS, AND HYPERCALCEMIA. N ENGL J MED 2016 AUG 11;375(6):567-74. 66.00 YR M Y 0.00000 20160907 MD US US

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
127216061 12721606 1 PS HYDROCHLOROTHIAZIDE. HYDROCHLOROTHIAZIDE 1 U 40807
127216061 12721606 2 SS IBUPROFEN. IBUPROFEN 1 U 0
127216061 12721606 3 SS ASPIRIN. ASPIRIN 1 U 0
127216061 12721606 4 SS CALCIUM CARBONATE. CALCIUM CARBONATE 1 U 0
127216061 12721606 5 SS NAPROXEN. NAPROXEN 1 U 0
127216061 12721606 6 SS ACETAMINOPHEN. ACETAMINOPHEN 1 U 0
127216061 12721606 7 C Tadalafil TADALAFIL 1 0
127216061 12721606 8 C Glucosamine GLUCOSAMINE 1 0
127216061 12721606 9 C DISULFIRAM. DISULFIRAM 1 0
127216061 12721606 10 C Tamsulosin TAMSULOSIN 1 0
127216061 12721606 11 C N-3 fatty acids 2 0
127216061 12721606 12 C Cyclobenzaprine CYCLOBENZAPRINE 1 0
127216061 12721606 13 C VITAMIN D CHOLECALCIFEROL 1 0
127216061 12721606 14 C AMLODIPINE AMLODIPINE BESYLATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127216061 12721606 1 Dyspepsia
127216061 12721606 2 Musculoskeletal discomfort
127216061 12721606 3 Dyspepsia
127216061 12721606 4 Dyspepsia
127216061 12721606 5 Musculoskeletal disorder
127216061 12721606 6 Musculoskeletal discomfort
127216061 12721606 8 Musculoskeletal disorder
127216061 12721606 10 Musculoskeletal disorder
127216061 12721606 11 Musculoskeletal disorder
127216061 12721606 13 Mineral supplementation

Outcome of event

Event ID CASEID OUTC COD
127216061 12721606 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127216061 12721606 Acute kidney injury
127216061 12721606 Condition aggravated
127216061 12721606 Hypercalcaemia
127216061 12721606 Milk-alkali syndrome

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found