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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
8610866 | 8746584 | I | 8610866-7 | 20100525 | 20100722 | 20120423 | PER | PHHY2010US34984 | NOVARTIS PHARMACEUTICALS CORP. | 53 | YR | F | N | 86 | KG | 20101118 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
8610866 | 1020670296 | C | SYNTHROID | 1 | |||||||
8610866 | 1020670294 | C | METHOTREXAT (METHOTREXATE) | 2 | |||||||
8610866 | 1020670298 | C | LITHIUM CARBONATE | 1 | |||||||
8610866 | 1020622457 | PS | FEMARA | 1 | Y | D | 20726 | ||||
8610866 | 1020670295 | C | LISINOPRIL | 1 |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
8610866 | OT |
Reactions reported
Event ID | PT |
---|---|
8610866 | ARTHRALGIA |
8610866 | ARTHRITIS |
8610866 | MYALGIA |
8610866 | MUSCLE SWELLING |
8610866 | SWELLING |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
8610866 | CSM |
Therapies reported
Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|
8610866 | 1020622457 | 20100507 | 20100525 |