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 |