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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 7064231 | 7993835 | I | 7064231-7 | 20101013 | 20101027 | EXP | DE-RANBAXY-2010RR-38879 | RANBAXYUS | YR | M | Y | 140 | KG | 20101027 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 7064231 | 1014974821 | SS | AMLODIPINE BESYLATE AND VALSARTAN | 1 | UNK | ||||||
| 7064231 | 1014974820 | PS | AMLODIPINE | 1 | 10 MG, UNK | 077974 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 7064231 | 1014974821 | HYPERTENSION |
| 7064231 | 1014974820 | HYPERTENSION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 7064231 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 7064231 | HAEMOLYTIC ANAEMIA |
| 7064231 | DRUG INTERACTION |
| 7064231 | DRUG ADMINISTRATION ERROR |
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 |
|---|---|---|---|---|---|
| 7064231 | 1014974821 | 20100804 |