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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126869722 | 12686972 | 2 | F | 20160823 | 20160826 | 20160906 | EXP | GB-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-122327 | RANBAXY | 0.00 | F | Y | 0.00000 | 20160906 | OT | GB | GB |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126869722 | 12686972 | 1 | PS | ANASTROZOLE. | ANASTROZOLE | 1 | Unknown | UNK | Y | U | 91177 | ||||||||
126869722 | 12686972 | 2 | SS | ANASTROZOLE. | ANASTROZOLE | 1 | Unknown | UNK | Y | U | 91177 | ||||||||
126869722 | 12686972 | 3 | SS | ANASTROZOLE. | ANASTROZOLE | 1 | Unknown | UNK | Y | U | 91177 | ||||||||
126869722 | 12686972 | 4 | SS | ANASTROZOLE. | ANASTROZOLE | 1 | Unknown | UNK | Y | U | 91177 | ||||||||
126869722 | 12686972 | 5 | SS | ANASTROZOLE. | ANASTROZOLE | 1 | Unknown | UNK | Y | U | 91177 | ||||||||
126869722 | 12686972 | 6 | SS | ACCORD HEALTHCARE ANASTROZOLE | ANASTROZOLE | 1 | Unknown | UNK | Y | U | 0 | ||||||||
126869722 | 12686972 | 7 | SS | ARIMIDEX | ANASTROZOLE | 1 | Unknown | UNK | Y | U | 0 | ||||||||
126869722 | 12686972 | 8 | C | OMEPRAZOLE. | OMEPRAZOLE | 1 | Unknown | FEW MONTHS | U | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126869722 | 12686972 | 1 | Product used for unknown indication |
126869722 | 12686972 | 6 | Product used for unknown indication |
126869722 | 12686972 | 7 | Product used for unknown indication |
126869722 | 12686972 | 8 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126869722 | 12686972 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126869722 | 12686972 | Abasia | |
126869722 | 12686972 | Adverse drug reaction | |
126869722 | 12686972 | Anxiety | |
126869722 | 12686972 | Confusional state | |
126869722 | 12686972 | Disability | |
126869722 | 12686972 | Discomfort | |
126869722 | 12686972 | Drug hypersensitivity | |
126869722 | 12686972 | Drug intolerance | |
126869722 | 12686972 | Drug level increased | |
126869722 | 12686972 | Emotional distress | |
126869722 | 12686972 | Fear | |
126869722 | 12686972 | Hernia | |
126869722 | 12686972 | Lip swelling | |
126869722 | 12686972 | Menopausal symptoms | |
126869722 | 12686972 | Mental disorder | |
126869722 | 12686972 | Movement disorder | |
126869722 | 12686972 | Muscle disorder | |
126869722 | 12686972 | Muscle tightness | |
126869722 | 12686972 | Overdose | |
126869722 | 12686972 | Paraesthesia oral | |
126869722 | 12686972 | Product substitution issue | |
126869722 | 12686972 | Speech disorder | |
126869722 | 12686972 | Stress | |
126869722 | 12686972 | Swollen tongue | |
126869722 | 12686972 | Withdrawal syndrome |
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 |
---|---|---|---|---|---|---|
126869722 | 12686972 | 1 | 2012 | 2013 | 0 | |
126869722 | 12686972 | 2 | 201305 | 201402 | 0 | |
126869722 | 12686972 | 6 | 201305 | 201305 | 0 | |
126869722 | 12686972 | 8 | 2012 | 2013 | 0 |