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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5195443 | 6206055 | I | 5195443-5 | 20061220 | 20061220 | 20061230 | EXP | CA-ABBOTT-06P-028-0354205-00 | ABBOTT | F | Y | 72.64 | KG | 20061230 | OT | CANADA |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5195443 | 1007999463 | PS | HUMIRA | 1 | SUBCUTANEOUS | 413569A04 | |||||
5195443 | 1007999464 | C | MINOCYCLINE HCL | 1 | |||||||
5195443 | 1007999465 | C | HYDROXYCHLOROQUINE PHOSPHATE | 2 | ORAL | ||||||
5195443 | 1007999466 | C | ERGOCALCIFEROL | 2 | ORAL | ||||||
5195443 | 1007999467 | C | CALCIUM | 2 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
5195443 | 1007999463 | RHEUMATOID ARTHRITIS |
5195443 | 1007999464 | DRUG USE FOR UNKNOWN INDICATION |
5195443 | 1007999465 | RHEUMATOID ARTHRITIS |
5195443 | 1007999466 | DRUG USE FOR UNKNOWN INDICATION |
5195443 | 1007999467 | DRUG USE FOR UNKNOWN INDICATION |
Outcome of event
Event ID | OUTC COD |
---|---|
5195443 | OT |
Reactions reported
Event ID | PT |
---|---|
5195443 | HYPERSENSITIVITY |
5195443 | THROAT TIGHTNESS |
5195443 | UNDERDOSE |
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 |
---|---|---|---|---|---|
5195443 | 1007999463 | 20061220 | 20061220 |