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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6387686 | 7139515 | F | 1 | 6387686-X | 20090101 | 20090918 | 20090930 | EXP | 8051829 | UCB, INC. | 53 | YR | F | N | 90.7 | KG | 20090928 | CN | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6387686 | 1012374644 | PS | CIMZIA | 1 | SUBCUTANEOUS | 400 MG SC | D | D | |||
6387686 | 1012429624 | C | LIPITOR | 1 | |||||||
6387686 | 1012429625 | C | ZYRTEC | 1 | |||||||
6387686 | 1012429627 | C | LEXAPRO | 1 | |||||||
6387686 | 1012429628 | C | TRAZODONE | 2 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6387686 | 1012374644 | CROHN'S DISEASE |
Outcome of event
Event ID | OUTC COD |
---|---|
6387686 | HO |
Reactions reported
Event ID | PT |
---|---|
6387686 | AGEUSIA |
6387686 | ANOSMIA |
6387686 | ASTHENOPIA |
6387686 | DIARRHOEA |
6387686 | DRUG INEFFECTIVE |
6387686 | DRY EYE |
6387686 | DYSGEUSIA |
6387686 | HERNIA HIATUS REPAIR |
6387686 | WEIGHT DECREASED |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
6387686 | CSM |
Therapies reported
Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|
6387686 | 1012374644 | 20090714 |