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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125404485 | 12540448 | 5 | F | 20160819 | 20160708 | 20160824 | PER | US-PFIZER INC-2016334875 | PFIZER | 53.00 | YR | F | Y | 68.00000 | KG | 20160824 | CN | US | US |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125404485 | 12540448 | 1 | SS | ENBREL | ETANERCEPT | 1 | SHOT, IN HER THIGH | Y | 0 | ||||||||||
125404485 | 12540448 | 2 | PS | SULFASALAZINE. | SULFASALAZINE | 1 | UNK | Y | 7073 | ||||||||||
125404485 | 12540448 | 3 | C | PREMPRO | ESTROGENS, CONJUGATEDMEDROXYPROGESTERONE ACETATE | 1 | Oral | UNK, 1X/DAY | 0 | TABLET | QD | ||||||||
125404485 | 12540448 | 4 | C | OMEPRAZOLE. | OMEPRAZOLE | 1 | Oral | 20 MG, 1X/DAY | 0 | 20 | MG | CAPSULE | QD | ||||||
125404485 | 12540448 | 5 | C | DICLOFENAC | DICLOFENAC | 1 | Oral | 75 MG, 1X/DAY | 0 | 75 | MG | TABLET | QD | ||||||
125404485 | 12540448 | 6 | C | CITALOPRAM | CITALOPRAM HYDROBROMIDE | 1 | Oral | 20 MG, 1X/DAY | 0 | 20 | MG | TABLET | QD | ||||||
125404485 | 12540448 | 7 | C | SUMATRIPTAN. | SUMATRIPTAN | 1 | Oral | 100 MG, AS NEEDED | 0 | 100 | MG | TABLET |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125404485 | 12540448 | 3 | Hormone therapy |
125404485 | 12540448 | 4 | Gastrooesophageal reflux disease |
125404485 | 12540448 | 5 | Rheumatoid arthritis |
125404485 | 12540448 | 6 | Depression |
125404485 | 12540448 | 7 | Migraine |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125404485 | 12540448 | Drug hypersensitivity | |
125404485 | 12540448 | Pain | |
125404485 | 12540448 | Pruritus | |
125404485 | 12540448 | Swelling | |
125404485 | 12540448 | Urticaria |
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 |
---|---|---|---|---|---|---|
125404485 | 12540448 | 1 | 201606 | 0 |