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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 8479472 | 8644123 | I | 8479472-1 | 20120626 | 20120629 | EXP | DE-PFIZER INC-2012154126 | PFIZERINC | YR | F | Y | 20120629 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 8479472 | 1020131666 | I | AMLODIPINE | 2 | 10 MG, UNK | ||||||
| 8479472 | 1020131665 | PS | ALPRAZOLAM | 1 | 1 OR 1.5 MG, DAILY | 018276 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 8479472 | 1020131666 | HYPERTENSION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 8479472 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 8479472 | SYNCOPE |
| 8479472 | DRUG INTERACTION |
| 8479472 | SKELETAL INJURY |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |