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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125522612 | 12552261 | 2 | F | 20160707 | 20160713 | 20160721 | EXP | ZA-CONCORDIA PHARMACEUTICALS INC.-GSH201607-003560 | CONCORDIA | MOUTON J,NJUGUNA C,KRAMER N,STEWART A,MEHTA U,COHEN K. ADVERSE DRUG REACTIONS CAUSING ADMISSION TO MEDICAL WARDS: A CROSS-SECTIONAL SURVEY AT 4 HOSPITALS IN SOUTH AFRICA. MEDICINE 2016 MAY;95(19):1-10. | 56.00 | YR | F | Y | 0.00000 | 20160721 | OT | ZA | ZA |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125522612 | 12552261 | 1 | SS | HYDRALAZINE | HYDRALAZINE HYDROCHLORIDE | 1 | Unknown | U | 0 | ||||||||||
125522612 | 12552261 | 2 | PS | Metoprolol Hydrochlorothiazide | HYDROCHLOROTHIAZIDEMETOPROLOL TARTRATE | 1 | Unknown | U | 21956 | ||||||||||
125522612 | 12552261 | 3 | SS | AMLODIPINE | AMLODIPINE BESYLATE | 1 | Unknown | U | 0 | ||||||||||
125522612 | 12552261 | 4 | SS | ATENOLOL. | ATENOLOL | 1 | Unknown | U | 0 | ||||||||||
125522612 | 12552261 | 5 | SS | Enalapril | ENALAPRIL | 1 | Unknown | U | 0 | ||||||||||
125522612 | 12552261 | 6 | SS | FUROSEMIDE. | FUROSEMIDE | 1 | Unknown | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125522612 | 12552261 | 1 | Product used for unknown indication |
125522612 | 12552261 | 2 | Product used for unknown indication |
125522612 | 12552261 | 3 | Product used for unknown indication |
125522612 | 12552261 | 4 | Product used for unknown indication |
125522612 | 12552261 | 5 | Product used for unknown indication |
125522612 | 12552261 | 6 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125522612 | 12552261 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125522612 | 12552261 | Renal impairment |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |