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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6699476 | 7368227 | F | 6699476-9 | 20080403 | 20100427 | 20100427 | EXP | CA-GENENTECH-259806 | GNEFDAAERSPRD | 37 | YR | F | Y | 95.2 | KG | 20100427 | CN | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6699476 | 1013580979 | PS | XOLAIR | 1 | SUBCUTANEOUS | 450 MG, Q2W | UNKNOWN | ||||
6699476 | 1013580980 | SS | XOLAIR | 1 | SUBCUTANEOUS | 450 MG, Q2W | S0079 | ||||
6699476 | 1013580981 | SS | XOLAIR | 1 | SUBCUTANEOUS | 450 MG, Q2W | S0079A | ||||
6699476 | 1013580982 | C | BENADRYL | 1 | |||||||
6699476 | 1013580983 | C | CORTISONE | 2 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6699476 | 1013580979 | ASTHMA |
6699476 | 1013580982 | IODINE ALLERGY |
6699476 | 1013580983 | IODINE ALLERGY |
Outcome of event
Event ID | OUTC COD |
---|---|
6699476 | OT |
Reactions reported
Event ID | PT |
---|---|
6699476 | ANXIETY |
6699476 | CYANOSIS |
6699476 | HEADACHE |
6699476 | HYPERSENSITIVITY |
6699476 | HYPERTENSION |
6699476 | SWELLING FACE |
6699476 | WEIGHT INCREASED |
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 |
---|---|---|---|---|---|
6699476 | 1013580979 | 20051111 | |||
6699476 | 1013580980 | 20100330 | |||
6699476 | 1013580981 | 20100413 |