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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126462252 | 12646225 | 2 | F | 20160729 | 20160811 | 20160812 | EXP | GB-JNJFOC-20160726957 | JOHNSON AND JOHNSON | 87.00 | YR | E | M | Y | 0.00000 | 20160812 | OT | GB | GB |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126462252 | 12646225 | 1 | PS | IBUPROFEN. | IBUPROFEN | 1 | Unknown | Y | N | 19012 | UNSPECIFIED | ||||||||
| 126462252 | 12646225 | 2 | SS | IBUPROFEN. | IBUPROFEN | 1 | Unknown | Y | N | 19012 | UNSPECIFIED | ||||||||
| 126462252 | 12646225 | 3 | SS | FUROSEMIDE. | FUROSEMIDE | 1 | Unknown | 40 DOSES (UNIT UNSPECIFIED) CHANGED TO INTRAVENOUS USE AFTER SUSPECT REACTION | Y | 0 | 40 | DF | UNSPECIFIED | ||||||
| 126462252 | 12646225 | 4 | C | RANITIDINE. | RANITIDINE | 1 | Unknown | 0 | UNSPECIFIED | ||||||||||
| 126462252 | 12646225 | 5 | C | ADCAL D3 | CALCIUM CARBONATECHOLECALCIFEROL | 1 | Unknown | 0 | UNSPECIFIED | ||||||||||
| 126462252 | 12646225 | 6 | C | SIMVASTATIN. | SIMVASTATIN | 1 | Unknown | 0 | UNSPECIFIED |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126462252 | 12646225 | 2 | Product used for unknown indication |
| 126462252 | 12646225 | 3 | Product used for unknown indication |
| 126462252 | 12646225 | 4 | Product used for unknown indication |
| 126462252 | 12646225 | 5 | Product used for unknown indication |
| 126462252 | 12646225 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126462252 | 12646225 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126462252 | 12646225 | Acute kidney injury | |
| 126462252 | 12646225 | Malaise |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |