Person who experienced the adverse event (patient)
| Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 7065351 | 7993836 | I | 7065351-3 | 20101015 | 20101027 | EXP | DE-WATSON-2010-14052 | WATSON | YR | M | Y | 140 | KG | 20101027 | CN | GERMANY |
Drug(s) used by person
| Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 7065351 | 1014979682 | SS | VALSARTAN | 1 | UNK | ||||||
| 7065351 | 1014979681 | SS | AMLODIPINE BESYLATE AND VALSARTAN | 1 | UNK | ||||||
| 7065351 | 1014979680 | PS | AMLODIPINE BESYLATE | 1 | UNK | UNCONFIRMED | 077671 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 7065351 | 1014979682 | HYPERTENSION |
| 7065351 | 1014979681 | HYPERTENSION |
| 7065351 | 1014979680 | HYPERTENSION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 7065351 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 7065351 | DRUG ADMINISTRATION ERROR |
| 7065351 | HAEMOLYTIC ANAEMIA |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 7065351 | 1014979681 | 20100804 |