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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
7586239 | 8030129 | I | 7586239-5 | 20110627 | 20110630 | DIR | 46 | YR | F | N | 20110628 | PH | N | N | UNITED STATES |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
7586239 | 1016915260 | PS | COPAXONE | 1 | 20 MG DAILY SQ |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
7586239 | 1016915260 | MULTIPLE SCLEROSIS |
Outcome of event
no results found |
Reactions reported
Event ID | PT |
---|---|
7586239 | URTICARIA |
7586239 | INJECTION SITE REACTION |
7586239 | CHEST DISCOMFORT |
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 |
---|---|---|---|---|---|
7586239 | 1016915260 | 20101011 |