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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 7205770 | 7832928 | I | 7205770-5 | 20100201 | 20101223 | 20101231 | EXP | CHPA2010US19571 | NOVARTIS CONSUMER HEALTH, INC. | 51 | YR | M | Y | 95.238 | KG | 20101231 | UNITED STATES |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 7205770 | 1015450437 | PS | PREVACID 24 HR | 1 | UNK, UNK | 022327 | |||||
| 7205770 | 1015450438 | SS | PREVACID 24 HR | 1 | 022327 | ||||||
| 7205770 | 1015450439 | SS | CELEBREX | 1 | ORAL | UNK, UNK | |||||
| 7205770 | 1015450440 | SS | RANITIDINE | 1 | UNK, UNK | ||||||
| 7205770 | 1015450441 | SS | RANITIDINE | 1 | |||||||
| 7205770 | 1015450442 | SS | VIAGRA | 1 | 100 MG, UNK |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 7205770 | 1015450437 | GASTROOESOPHAGEAL REFLUX DISEASE |
| 7205770 | 1015450438 | HERNIA |
| 7205770 | 1015450439 | ARTHRITIS |
| 7205770 | 1015450440 | HERNIA |
| 7205770 | 1015450441 | GASTROOESOPHAGEAL REFLUX DISEASE |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 7205770 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 7205770 | GASTRIC DISORDER |
| 7205770 | GASTRIC OPERATION |
| 7205770 | KNEE OPERATION |
| 7205770 | MALAISE |
| 7205770 | OEDEMA PERIPHERAL |
| 7205770 | OFF LABEL USE |
| 7205770 | SKIN DISCOLOURATION |
| 7205770 | ULCER |
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 |
|---|---|---|---|---|---|
| 7205770 | 1015450439 | 20100201 |