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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
8479196 | 8643969 | I | 8479196-0 | 20111101 | 20120618 | 20120629 | EXP | DE-TEVA-332418GER | TEVA | 35 | YR | F | Y | 62 | KG | 20120629 | MD | GERMANY |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
8479196 | 1020130595 | PS | COPAXONE | 1 | SUBCUTANEOUS | 20 MILLIGRAM; | 020622 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
8479196 | 1020130595 | MULTIPLE SCLEROSIS |
Outcome of event
Event ID | OUTC COD |
---|---|
8479196 | HO |
Reactions reported
Event ID | PT |
---|---|
8479196 | ABDOMINAL ADHESIONS |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|
8479196 | 1020130595 | 20110925 |