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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5460361 | 6423328 | I | 5460361-1 | 20070302 | 20070402 | PER | LIT-001-07-US | OCTAPHARMA USA | 29 | YR | F | N | 20070302 | OT | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5460361 | 1008949323 | PS | IMMUNE GLOBULIN INTRAVENOUS (HUMAN) | 1 | OVER 3DAYS |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
5460361 | 1008949323 | MYOPATHY |
Outcome of event
Event ID | OUTC COD |
---|---|
5460361 | HO |
Reactions reported
Event ID | PT |
---|---|
5460361 | MENINGITIS ASEPTIC |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
5460361 | LIT |
Therapies reported
no results found |