Person who experienced the adverse event (patient)
| Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126079941 | 12607994 | 1 | I | 20160712 | 20160729 | 20160729 | EXP | US-JNJFOC-20160722903 | JANSSEN | 0.00 | M | Y | 0.00000 | 20160729 | CN | US | US |
Drug(s) used by person
| Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126079941 | 12607994 | 1 | PS | TRAMADOL HYDROCHLORIDE. | TRAMADOL HYDROCHLORIDE | 1 | Oral | U | U | 20281 | 50 | MG | UNSPECIFIED | Q6H | |||||
| 126079941 | 12607994 | 2 | SS | LYRICA | PREGABALIN | 1 | Oral | UNKNOWN | 0 | 100 | MG | CAPSULE | BID | ||||||
| 126079941 | 12607994 | 3 | C | VITAMINE B1 | 2 | Oral | 0 | 1 | DF | UNSPECIFIED | QD | ||||||||
| 126079941 | 12607994 | 4 | C | PANTOPRAZOLE SODIUM. | PANTOPRAZOLE SODIUM | 1 | Unknown | 0 | 40 | MG | UNSPECIFIED | ||||||||
| 126079941 | 12607994 | 5 | C | PANTOPRAZOLE SODIUM. | PANTOPRAZOLE SODIUM | 1 | Unknown | 0 | UNSPECIFIED | ||||||||||
| 126079941 | 12607994 | 6 | C | PANTOPRAZOLE SODIUM. | PANTOPRAZOLE SODIUM | 1 | Unknown | 0 | 40 | MG | UNSPECIFIED | ||||||||
| 126079941 | 12607994 | 7 | C | PANTOPRAZOLE SODIUM. | PANTOPRAZOLE SODIUM | 1 | Unknown | 0 | UNSPECIFIED |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126079941 | 12607994 | 1 | Musculoskeletal pain |
| 126079941 | 12607994 | 2 | Nerve injury |
| 126079941 | 12607994 | 3 | Unevaluable therapy |
| 126079941 | 12607994 | 4 | Nausea |
| 126079941 | 12607994 | 5 | Nausea |
| 126079941 | 12607994 | 6 | Nausea |
| 126079941 | 12607994 | 7 | Nausea |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126079941 | 12607994 | OT |
| 126079941 | 12607994 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126079941 | 12607994 | General physical health deterioration | |
| 126079941 | 12607994 | Haematemesis | |
| 126079941 | 12607994 | Hepatic cirrhosis | |
| 126079941 | 12607994 | Hepatitis C | |
| 126079941 | 12607994 | Internal haemorrhage | |
| 126079941 | 12607994 | Somnolence |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |