Person who experienced the adverse event (patient)
Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
119833922 | 11983392 | 2 | F | 2010 | 20160715 | 20160201 | 20160726 | EXP | BR-ABBVIE-16K-020-1545845-00 | ABBVIE | 56.97 | YR | F | Y | 69.00000 | KG | 20160726 | CN | COUNTRY NOT SPECIFIED | BR |
Drug(s) used by person
Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
119833922 | 11983392 | 1 | PS | HUMIRA | ADALIMUMAB | 1 | Subcutaneous | Y | 51072XH01 | 125057 | 40 | MG | SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE | ||||||
119833922 | 11983392 | 2 | SS | HUMIRA | ADALIMUMAB | 1 | Subcutaneous | Y | 51072XH01 | 125057 | 40 | MG | SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE | ||||||
119833922 | 11983392 | 3 | C | SULFASALAZINE. | SULFASALAZINE | 1 | Oral | 0 | TABLET | ||||||||||
119833922 | 11983392 | 4 | C | PREDNISONE. | PREDNISONE | 1 | Oral | 0 | TABLET | ||||||||||
119833922 | 11983392 | 5 | C | SIMVASTATIN. | SIMVASTATIN | 1 | Oral | 0 | TABLET | ||||||||||
119833922 | 11983392 | 6 | C | PROPRANOLOL | PROPRANOLOLPROPRANOLOL HYDROCHLORIDE | 1 | Oral | 0 | TABLET | ||||||||||
119833922 | 11983392 | 7 | C | INDAPAMIDE. | INDAPAMIDE | 1 | Oral | 0 | TABLET | ||||||||||
119833922 | 11983392 | 8 | C | AMITRIPTYLINE | AMITRIPTYLINE | 1 | Oral | 0 | TABLET | ||||||||||
119833922 | 11983392 | 9 | C | DIAZEPAM. | DIAZEPAM | 1 | Oral | 0 | TABLET | ||||||||||
119833922 | 11983392 | 10 | C | VITAMIN D/CALCIUM | CALCIUMVITAMIN D | 1 | Oral | 0 | TABLET | ||||||||||
119833922 | 11983392 | 11 | C | ALENDRONATE | ALENDRONATE SODIUM | 1 | Oral | 0 | 1 | DF | TABLET | /wk | |||||||
119833922 | 11983392 | 12 | C | OMEPRAZOLE. | OMEPRAZOLE | 1 | Oral | 0 | TABLET | ||||||||||
119833922 | 11983392 | 13 | C | CODEINE | CODEINE | 1 | Oral | 0 | TABLET | ||||||||||
119833922 | 11983392 | 14 | C | CODEINE | CODEINE | 1 | Oral | 0 | TABLET |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
119833922 | 11983392 | 1 | Rheumatoid arthritis |
119833922 | 11983392 | 3 | Rheumatic disorder |
119833922 | 11983392 | 4 | Pain |
119833922 | 11983392 | 5 | Blood cholesterol abnormal |
119833922 | 11983392 | 6 | Hypertension |
119833922 | 11983392 | 7 | Hypertension |
119833922 | 11983392 | 8 | Fibromyalgia |
119833922 | 11983392 | 9 | Pain |
119833922 | 11983392 | 10 | Bone disorder |
119833922 | 11983392 | 11 | Bone disorder |
119833922 | 11983392 | 12 | Gastric disorder |
119833922 | 11983392 | 13 | Spinal disorder |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
119833922 | 11983392 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
119833922 | 11983392 | Bone pain | |
119833922 | 11983392 | Fall | |
119833922 | 11983392 | Sinusitis | |
119833922 | 11983392 | Spinal osteoarthritis |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|---|
119833922 | 11983392 | 1 | 20090101 | 20151221 | 0 | |
119833922 | 11983392 | 3 | 2005 | 0 | ||
119833922 | 11983392 | 4 | 1999 | 0 | ||
119833922 | 11983392 | 5 | 2010 | 0 | ||
119833922 | 11983392 | 8 | 2008 | 0 | ||
119833922 | 11983392 | 9 | 2008 | 201605 | 0 | |
119833922 | 11983392 | 10 | 2004 | 0 | ||
119833922 | 11983392 | 11 | 2004 | 0 | ||
119833922 | 11983392 | 13 | 201410 | 0 | ||
119833922 | 11983392 | 14 | 201504 | 201606 | 0 |