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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6811419 | 7450032 | I | 6811419-3 | 20100618 | 20100630 | EXP | FR-GENENTECH-303333 | GNEFDAAERSPRD | YR | M | Y | 20100630 | OT | SWITZERLAND |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6811419 | 1014011649 | PS | XOLAIR | 1 | 375 MG, Q2W | NOT REPORTED |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6811419 | 1014011649 | ASTHMA |
Outcome of event
Event ID | OUTC COD |
---|---|
6811419 | OT |
Reactions reported
Event ID | PT |
---|---|
6811419 | AUTOIMMUNE THYROIDITIS |
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 |
---|---|---|---|---|---|
6811419 | 1014011649 | 20070101 |