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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126779691 | 12677969 | 1 | I | 201605 | 20160707 | 20160823 | 20160823 | EXP | PHHY2016AR096089 | NOVARTIS | 55.05 | YR | M | Y | 0.00000 | 20160823 | CN | COUNTRY NOT SPECIFIED | AR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126779691 | 12677969 | 1 | SS | EXFORGE | AMLODIPINE BESYLATEVALSARTAN | 1 | Unknown | 1.5 DF (VALSARTAN 160, AMLODIPINE 5), QD | U | 0 | 1.5 | DF | FILM-COATED TABLET | QD | |||||
| 126779691 | 12677969 | 2 | SS | EXFORGE | AMLODIPINE BESYLATEVALSARTAN | 1 | Unknown | 1 DF (VALSARTAN 160, AMLODIPINE 5), UNK | U | 0 | 1 | DF | FILM-COATED TABLET | QD | |||||
| 126779691 | 12677969 | 3 | PS | DIOVAN | VALSARTAN | 1 | Unknown | 0.5 DF (160 MG), QD | U | 21283 | .5 | DF | TABLET | QD | |||||
| 126779691 | 12677969 | 4 | C | AMLODIPINE | AMLODIPINE BESYLATE | 1 | 5 MG, QD | Y | 0 | 5 | MG | QD | |||||||
| 126779691 | 12677969 | 5 | C | ASPIRINE | ASPIRIN | 1 | Unknown | QD | U | 0 | QD | ||||||||
| 126779691 | 12677969 | 6 | C | ROSUVASTATIN. | ROSUVASTATIN | 1 | Unknown | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126779691 | 12677969 | 1 | Hypertension |
| 126779691 | 12677969 | 3 | Hypertension |
| 126779691 | 12677969 | 4 | Hypertension |
| 126779691 | 12677969 | 5 | Product used for unknown indication |
| 126779691 | 12677969 | 6 | Blood cholesterol abnormal |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126779691 | 12677969 | HO |
| 126779691 | 12677969 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126779691 | 12677969 | Angina pectoris | |
| 126779691 | 12677969 | Myalgia | |
| 126779691 | 12677969 | Syncope | |
| 126779691 | 12677969 | Wrong technique in product usage process |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |