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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125881962 | 12588196 | 2 | F | 20160728 | 20160725 | 20160803 | EXP | PHHY2016BR098698 | NOVARTIS | 0.00 | F | Y | 70.00000 | KG | 20160803 | MD | BR | BR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125881962 | 12588196 | 1 | PS | DIOVAN | VALSARTAN | 1 | Oral | 80 MG, QD | Y | 21283 | 80 | MG | TABLET | QD | |||||
| 125881962 | 12588196 | 2 | SS | DIOVAN | VALSARTAN | 1 | Oral | 80 MG, BID | Y | 21283 | 80 | MG | TABLET | BID | |||||
| 125881962 | 12588196 | 3 | SS | DIOVAN HCT | HYDROCHLOROTHIAZIDEVALSARTAN | 1 | Oral | 1 DF (HYDROCHLOROTHIAZIDE 25 MG, VALSARTAN 160 MG), QD (IN THE MORNING) | U | 0 | 1 | DF | TABLET | QD | |||||
| 125881962 | 12588196 | 4 | SS | ARIMIDEX | ANASTROZOLE | 1 | Oral | 1 DF, QD | U | 0 | 1 | DF | TABLET | QD | |||||
| 125881962 | 12588196 | 5 | C | SELOZOK | METOPROLOL SUCCINATE | 1 | Oral | 25 MG, QD | U | 0 | 25 | MG | TABLET | QD | |||||
| 125881962 | 12588196 | 6 | C | SELOZOK | METOPROLOL SUCCINATE | 1 | U | 0 | TABLET | ||||||||||
| 125881962 | 12588196 | 7 | C | FRONTAL | ALPRAZOLAM | 1 | Oral | 1.5 DF, QD (1 DF AT NIGHT AND 0.5 DF IN THE MORNING) | U | 0 | 1.5 | DF | TABLET | QD | |||||
| 125881962 | 12588196 | 8 | C | PARIET | RABEPRAZOLE SODIUM | 1 | Unknown | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125881962 | 12588196 | 1 | Hypertension |
| 125881962 | 12588196 | 3 | Hypertension |
| 125881962 | 12588196 | 4 | Breast cancer |
| 125881962 | 12588196 | 5 | Blood pressure abnormal |
| 125881962 | 12588196 | 6 | Heart rate irregular |
| 125881962 | 12588196 | 7 | Blood pressure abnormal |
| 125881962 | 12588196 | 8 | Prophylaxis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125881962 | 12588196 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125881962 | 12588196 | Abdominal pain upper | |
| 125881962 | 12588196 | Anxiety | |
| 125881962 | 12588196 | Blood pressure inadequately controlled | |
| 125881962 | 12588196 | Blood pressure increased | |
| 125881962 | 12588196 | Body height decreased | |
| 125881962 | 12588196 | Breast cancer | |
| 125881962 | 12588196 | Concomitant disease aggravated | |
| 125881962 | 12588196 | Depression | |
| 125881962 | 12588196 | Drug ineffective | |
| 125881962 | 12588196 | Irritability | |
| 125881962 | 12588196 | Malaise | |
| 125881962 | 12588196 | Osteoporosis |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |