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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 73105752 | 7310575 | 2 | F | 200906 | 20130919 | 20100310 | 20130930 | EXP | US-BIOGENIDEC-2010BI007070 | BIOGEN | 60.12 | YR | F | Y | 0.00000 | 20130930 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 73105752 | 7310575 | 1 | PS | AVONEX | 1 | INTRAMUSCULAR | D | 103628 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 73105752 | 7310575 | 1 | Multiple sclerosis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 73105752 | 7310575 | HO |
| 73105752 | 7310575 | DE |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 73105752 | 7310575 | Abdominal distension | |
| 73105752 | 7310575 | Asthenia | |
| 73105752 | 7310575 | Blood pressure decreased | |
| 73105752 | 7310575 | Diabetes mellitus | |
| 73105752 | 7310575 | Dyspnoea | |
| 73105752 | 7310575 | Fall | |
| 73105752 | 7310575 | Femur fracture | |
| 73105752 | 7310575 | Gait disturbance | |
| 73105752 | 7310575 | Pain | |
| 73105752 | 7310575 | Renal failure | |
| 73105752 | 7310575 | Rib fracture | |
| 73105752 | 7310575 | Urinary tract infection |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |