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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6524170 | 7235364 | I | 6524170-4 | 20091218 | 20091218 | 20091231 | PER | US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2009-BP-14632BP | B.I. PHARMACEUTICALS,INC./RIDGEFIELD | 28 | YR | F | Y | 20091231 | CN |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6524170 | 1012889271 | PS | ZANTAC 150 | 1 | ORAL | 150 MG | A48201 | 021698 | |||
| 6524170 | 1012889272 | C | NAPROXEN | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6524170 | 1012889271 | DYSPEPSIA |
| 6524170 | 1012889272 | PAIN |
Outcome of event
| no results found |
Reactions reported
| Event ID | PT |
|---|---|
| 6524170 | DRUG INEFFECTIVE |
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 |
|---|---|---|---|---|---|
| 6524170 | 1012889271 | 20091218 | |||
| 6524170 | 1012889272 | 20091211 |