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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 7403013 | 7908253 | I | 7403013-0 | 20101101 | 20110317 | 20110331 | EXP | AUR-APL-2011-01054 | AUROBINDO PHARMA USA | 76 | YR | F | N | 20110328 | OT |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 7403013 | 1016307640 | C | AMLODIPINE | 1 | |||||||
| 7403013 | 1016206948 | PS | LOSARTAN POTASSIUM | 1 | ORAL | ORAL | D | D | 090083 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 7403013 | 1016206948 | HYPERTENSION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 7403013 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 7403013 | PEMPHIGOID |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 7403013 | HP |
| 7403013 | FGN |
| 7403013 | OTH |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 7403013 | 1016206948 | 20100812 |