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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
118791062 | 11879106 | 2 | F | 20160920 | 20151230 | 20160930 | EXP | GB-MHRA-ADR 23282784 | GB-WEST-WARD PHARMACEUTICALS CORP.-GB-H14001-15-02203 | WESTWARD | 75.00 | YR | F | Y | 0.00000 | 20160930 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
118791062 | 11879106 | 1 | PS | FLUCONAZOLE. | FLUCONAZOLE | 1 | Unknown | 76736 | |||||||||||
118791062 | 11879106 | 2 | SS | EVEROLIMUS | EVEROLIMUS | 1 | Unknown | 0 | |||||||||||
118791062 | 11879106 | 3 | C | EXEMESTANE. | EXEMESTANE | 1 | Unknown | 0 | |||||||||||
118791062 | 11879106 | 4 | C | ANTIBIOTICS | UNSPECIFIED INGREDIENT | 1 | Unknown | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
118791062 | 11879106 | 1 | Cellulitis |
118791062 | 11879106 | 2 | Breast cancer metastatic |
118791062 | 11879106 | 3 | Breast cancer metastatic |
118791062 | 11879106 | 4 | Cellulitis |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
118791062 | 11879106 | DE |
118791062 | 11879106 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
118791062 | 11879106 | Diarrhoea | |
118791062 | 11879106 | Labelled drug-drug interaction medication error |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |