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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126100161 | 12610016 | 1 | I | 20160721 | 20160729 | 20160801 | 20160801 | EXP | IT-ROCHE-1806205 | ROCHE | 47.15 | YR | F | Y | 0.00000 | 20160801 | MD | IT | IT |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126100161 | 12610016 | 1 | PS | MABTHERA | RITUXIMAB | 1 | Intravenous (not otherwise specified) | Y | 143558 | 103705 | 1000 | MG | SOLUTION FOR INFUSION | ||||||
| 126100161 | 12610016 | 2 | C | RANITIDINE. | RANITIDINE | 1 | Intravenous (not otherwise specified) | 0 | 50 | MG | |||||||||
| 126100161 | 12610016 | 3 | C | BRUFEN | IBUPROFEN | 1 | Oral | 0 | 600 | MG | TABLET | ||||||||
| 126100161 | 12610016 | 4 | C | TRIMETON (ITALY) | 2 | Intravenous bolus | 10 MG/1 ML 5 X 1 ML VIALS | 0 | 10 | MG | |||||||||
| 126100161 | 12610016 | 5 | C | SOLU-MEDROL | METHYLPREDNISOLONE SODIUM SUCCINATE | 1 | Intravenous (not otherwise specified) | 0 | 125 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126100161 | 12610016 | 1 | Multiple sclerosis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126100161 | 12610016 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126100161 | 12610016 | Dysphonia | |
| 126100161 | 12610016 | Dyspnoea | |
| 126100161 | 12610016 | Erythema | |
| 126100161 | 12610016 | Laryngeal oedema | |
| 126100161 | 12610016 | Urticaria |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 126100161 | 12610016 | 1 | 20160721 | 20160721 | 0 |