Person who experienced the adverse event (patient)
Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5127243 | 5903287 | F | 1 | 5127243-6 | 20050901 | 20060929 | 20061010 | EXP | 2005BI017679 | BIOGEN IDEC INC. | 45 | YR | M | N | 120 | KG | 20061009 | MD | FRANCE |
Drug(s) used by person
Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
---|---|---|---|---|---|---|---|---|---|---|---|
5127243 | 1007757411 | PS | AVONEX | 1 | INTRAMUSCULAR | 30 UG; QW; IM | D | D |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
5127243 | 1007757411 | MULTIPLE SCLEROSIS |
Outcome of event
Event ID | OUTC COD |
---|---|
5127243 | HO |
Reactions reported
Event ID | PT |
---|---|
5127243 | ALCOHOLISM |
5127243 | ANXIETY |
5127243 | ASPARTATE AMINOTRANSFERASE INCREASED |
5127243 | BRAIN NATRIURETIC PEPTIDE INCREASED |
5127243 | BUNDLE BRANCH BLOCK LEFT |
5127243 | CARDIAC FAILURE ACUTE |
5127243 | CARDIOMEGALY |
5127243 | CARDIOMYOPATHY |
5127243 | GAMMA-GLUTAMYLTRANSFERASE INCREASED |
5127243 | HEPATOJUGULAR REFLUX |
5127243 | INSOMNIA |
5127243 | PRURIGO |
5127243 | RASH ERYTHEMATOUS |
5127243 | SINUS TACHYCARDIA |
5127243 | SKIN LESION |
5127243 | VENTRICULAR HYPOKINESIA |
5127243 | WEIGHT INCREASED |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
5127243 | FGN |
5127243 | HP |
Therapies reported
Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|
5127243 | 1007757411 | 20031001 | 20050901 |