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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
4646879 | 5807418 | I | 4646879-X | 20050209 | 20050217 | 20050331 | PER | 05P-163-0291085-00 | PPD PHARMACOVIGILANCE | 78 | YR | F | N | 150 | LBS | 20050217 | OT |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
4646879 | 1005921176 | PS | HUMIRA | 1 | SUBCUTANEOUS | 40 MG, 1 IN 2 WK, SUBCUTANEOUS | D | D | |||
4646879 | 1006054616 | C | PREDNISONE | 1 | |||||||
4646879 | 1006054617 | C | METHOTREXATE | 2 | |||||||
4646879 | 1006054618 | C | HYDROXYCHLOROQUINE PHOSPHATE | 2 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
4646879 | 1005921176 | RHEUMATOID ARTHRITIS |
Outcome of event
no results found |
Reactions reported
Event ID | PT |
---|---|
4646879 | FATIGUE |
4646879 | JOINT SWELLING |
4646879 | WEIGHT INCREASED |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
4646879 | CSM |
4646879 | HP |
Therapies reported
Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|
4646879 | 1005921176 | 20050112 |