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
127097613 12709761 3 F 20160902 20160902 20160916 EXP US-DRREDDYS-USA/USA/16/0082908 DR REDDYS 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;375(6):567-74. 66.00 YR M Y 0.00000 20160916 MD COUNTRY NOT SPECIFIED 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
127097613 12709761 1 PS IBUPROFEN. IBUPROFEN 1 Unknown U U UNKNOWN 75682
127097613 12709761 2 SS NAPROXEN. NAPROXEN 1 Unknown U U UNKNOWN 78486
127097613 12709761 3 SS paracetamol ACETAMINOPHEN 1 Unknown 0
127097613 12709761 4 SS acetylsalicylic acid ASPIRIN 1 Unknown 0
127097613 12709761 5 SS CALCIUM CARBONATE. CALCIUM CARBONATE 1 Unknown Y 0
127097613 12709761 6 SS HYDROCHLOROTHIAZIDE. HYDROCHLOROTHIAZIDE 1 Unknown Y 0
127097613 12709761 7 C DISULFIRAM. DISULFIRAM 1 Unknown 0
127097613 12709761 8 C AMLODIPINE AMLODIPINE BESYLATE 1 Unknown 0
127097613 12709761 9 C tamsulosin TAMSULOSIN 1 Unknown 0
127097613 12709761 10 C VITAMIN D CHOLECALCIFEROL 1 Unknown 0
127097613 12709761 11 C glucosamine GLUCOSAMINE 1 Unknown 0
127097613 12709761 12 C tadalafil TADALAFIL 1 Unknown 0
127097613 12709761 13 C cyclobenzaprine CYCLOBENZAPRINE 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127097613 12709761 1 Musculoskeletal discomfort
127097613 12709761 2 Musculoskeletal discomfort
127097613 12709761 3 Musculoskeletal discomfort
127097613 12709761 4 Product used for unknown indication
127097613 12709761 5 Dyspepsia
127097613 12709761 6 Product used for unknown indication
127097613 12709761 7 Product used for unknown indication
127097613 12709761 8 Product used for unknown indication
127097613 12709761 9 Product used for unknown indication
127097613 12709761 10 Product used for unknown indication
127097613 12709761 11 Product used for unknown indication
127097613 12709761 12 Product used for unknown indication
127097613 12709761 13 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127097613 12709761 OT
127097613 12709761 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127097613 12709761 Acute kidney injury
127097613 12709761 Condition aggravated
127097613 12709761 Hypercalcaemia
127097613 12709761 Metabolic alkalosis
127097613 12709761 Milk-alkali syndrome
127097613 12709761 Overdose

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

no results found

Therapies reported

no results found