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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 113992233 | 11399223 | 3 | F | 20150811 | 20150820 | 20160809 | PER | US-ACTAVIS-2015-17208 | ACTAVIS | 0.00 | F | Y | 0.00000 | 20160809 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 113992233 | 11399223 | 1 | PS | PROPRANOLOL | PROPRANOLOLPROPRANOLOL HYDROCHLORIDE | 1 | UNKNOWN | U | UNKNOWN | 78494 | |||||||||
| 113992233 | 11399223 | 2 | SS | Anastrozole (Watson Laboratories) | ANASTROZOLE | 1 | Unknown | UNKNOWN | U | UNKNOWN | 0 | UNK | |||||||
| 113992233 | 11399223 | 3 | SS | LOSORTAN POTASSIUM | LOSARTAN POTASSIUM | 1 | Unknown | UNKNOWN | U | UNKNOWN | 0 | UNK | |||||||
| 113992233 | 11399223 | 4 | SS | Tamoxifen Citrate (Actavis Laboratories FL) | TAMOXIFEN CITRATE | 1 | Unknown | UNKNOWN | U | UNKNOWN | 0 | UNK | |||||||
| 113992233 | 11399223 | 5 | SS | Diltiazem HCL ER (LA) (Actavis Laboratories FL) | DILTIAZEM HYDROCHLORIDE | 1 | Unknown | UNKNOWN | U | UNKNOWN | 0 | TABLET (EXTENDED RELEASE) | |||||||
| 113992233 | 11399223 | 6 | SS | Metoprolol Succinate (Actavis Laboratories FL) | METOPROLOL SUCCINATE | 1 | Unknown | UNKNOWN | U | UNKNOWN | 0 | UNK |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 113992233 | 11399223 | 1 | Product used for unknown indication |
| 113992233 | 11399223 | 2 | Product used for unknown indication |
| 113992233 | 11399223 | 3 | Product used for unknown indication |
| 113992233 | 11399223 | 4 | Product used for unknown indication |
| 113992233 | 11399223 | 5 | Product used for unknown indication |
| 113992233 | 11399223 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 113992233 | 11399223 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 113992233 | 11399223 | Bone pain | |
| 113992233 | 11399223 | Cardiac failure congestive | |
| 113992233 | 11399223 | Diarrhoea | |
| 113992233 | 11399223 | Drug hypersensitivity |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |