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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
926736310 | 9267363 | 10 | F | 1995 | 20160913 | 20130502 | 20160921 | EXP | US-ASTRAZENECA-2011SE68502 | ASTRAZENECA | 81.00 | YR | F | Y | 56.20000 | KG | 20160921 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
926736310 | 9267363 | 1 | PS | ARIMIDEX | ANASTROZOLE | 1 | Oral | 20541 | TABLET | ||||||||||
926736310 | 9267363 | 2 | SS | ARIMIDEX | ANASTROZOLE | 1 | Oral | 20541 | TABLET | ||||||||||
926736310 | 9267363 | 3 | SS | ARIMIDEX | ANASTROZOLE | 1 | Unknown | GENERIC | 20541 | ||||||||||
926736310 | 9267363 | 4 | SS | ARIMIDEX | ANASTROZOLE | 1 | Oral | 20541 | 1 | MG | TABLET | QD | |||||||
926736310 | 9267363 | 5 | SS | ARIMIDEX | ANASTROZOLE | 1 | Oral | 20541 | 1 | MG | TABLET | QD | |||||||
926736310 | 9267363 | 6 | SS | PRILOSEC | OMEPRAZOLE MAGNESIUM | 1 | Oral | U | 0 | ||||||||||
926736310 | 9267363 | 7 | SS | TAMOXIFEN | TAMOXIFEN | 1 | Oral | Y | U | 0 | TABLET | ||||||||
926736310 | 9267363 | 8 | C | AREDIA | PAMIDRONATE DISODIUM | 1 | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
926736310 | 9267363 | 1 | Breast cancer female |
926736310 | 9267363 | 2 | Breast cancer female |
926736310 | 9267363 | 3 | Breast cancer female |
926736310 | 9267363 | 4 | Breast cancer female |
926736310 | 9267363 | 5 | Breast cancer female |
926736310 | 9267363 | 7 | Recurrent cancer |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
926736310 | 9267363 | HO |
926736310 | 9267363 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
926736310 | 9267363 | Anxiety | |
926736310 | 9267363 | Asthenia | |
926736310 | 9267363 | Autoimmune haemolytic anaemia | |
926736310 | 9267363 | Blood bilirubin increased | |
926736310 | 9267363 | Blood test abnormal | |
926736310 | 9267363 | Body height decreased | |
926736310 | 9267363 | Brucellosis | |
926736310 | 9267363 | Carbohydrate antigen 27.29 increased | |
926736310 | 9267363 | Carcinoembryonic antigen increased | |
926736310 | 9267363 | Drug dose omission | |
926736310 | 9267363 | Dyspnoea | |
926736310 | 9267363 | Fatigue | |
926736310 | 9267363 | Horner's syndrome | |
926736310 | 9267363 | Lymphadenopathy | |
926736310 | 9267363 | Malaise | |
926736310 | 9267363 | Malignant neoplasm progression | |
926736310 | 9267363 | Marrow hyperplasia | |
926736310 | 9267363 | Neck pain | |
926736310 | 9267363 | Pain | |
926736310 | 9267363 | Peptic ulcer | |
926736310 | 9267363 | Renal disorder |
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 |
---|---|---|---|---|---|---|
926736310 | 9267363 | 1 | 1998 | 0 | ||
926736310 | 9267363 | 2 | 2007 | 201202 | 0 | |
926736310 | 9267363 | 3 | 201202 | 0 | ||
926736310 | 9267363 | 4 | 2012 | 0 | ||
926736310 | 9267363 | 5 | 20160902 | 0 | ||
926736310 | 9267363 | 7 | 1998 | 0 |