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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 118700393 | 11870039 | 3 | F | 20160815 | 20151228 | 20160830 | PER | US-BAYER-2015-496452 | BAYER | 72.00 | YR | E | F | Y | 0.00000 | 20160830 | PH | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 118700393 | 11870039 | 1 | PS | BETASERON | INTERFERON BETA-1B | 1 | Subcutaneous | 0.3 MG 18 HOUR | 444145A | 103471 | .3 | MG | POWDER AND SOLVENT FOR SOLUTION FOR INJECTION | ||||||
| 118700393 | 11870039 | 2 | SS | BETASERON | INTERFERON BETA-1B | 1 | Subcutaneous | 0.3 MG, QOD | 52205A | 103471 | .3 | MG | POWDER AND SOLVENT FOR SOLUTION FOR INJECTION | QOD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 118700393 | 11870039 | 1 | Multiple sclerosis |
| 118700393 | 11870039 | 2 | Multiple sclerosis |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 118700393 | 11870039 | Drug dose omission | |
| 118700393 | 11870039 | Fall | |
| 118700393 | 11870039 | Hypoaesthesia | |
| 118700393 | 11870039 | Muscular weakness |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |