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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
4914423 | 5986151 | I | 4914423-5 | 20051212 | 20060206 | 20060216 | EXP | US-ABBOTT-06P-163-0324135-00 | ABBOTT | M | Y | 63.106 | KG | 20060216 | MD | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
4914423 | 1006944745 | PS | HUMIRA | 1 | SUBCUTANEOUS | UNKNOWN | |||||
4914423 | 1006944746 | C | LEVOTHYROXINE SODIUM | 1 | ORAL | ||||||
4914423 | 1006944747 | C | METHOTREXATE SODIUM | 1 | ORAL | 2.5MG TABS. 8 TABS 1/DAY/WK | |||||
4914423 | 1006944748 | C | SPIREVA INHALER | 2 | RESPIRATORY (INHALATION) | ||||||
4914423 | 1006944749 | C | SERETIDE MITE | 2 | RESPIRATORY (INHALATION) | ||||||
4914423 | 1006944750 | C | VITAMINS | 2 | ORAL |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
4914423 | 1006944745 | RHEUMATOID ARTHRITIS |
4914423 | 1006944746 | HYPOTHYROIDISM |
4914423 | 1006944747 | RHEUMATOID ARTHRITIS |
4914423 | 1006944748 | EMPHYSEMA |
4914423 | 1006944749 | EMPHYSEMA |
4914423 | 1006944750 | VITAMIN SUPPLEMENTATION |
Outcome of event
Event ID | OUTC COD |
---|---|
4914423 | HO |
Reactions reported
Event ID | PT |
---|---|
4914423 | FALL |
4914423 | PNEUMOTHORAX TRAUMATIC |
4914423 | RIB FRACTURE |
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 |
---|---|---|---|---|---|
4914423 | 1006944745 | 20050201 | |||
4914423 | 1006944748 | 20040101 | |||
4914423 | 1006944749 | 20040101 |