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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126053621 | 12605362 | 1 | I | 20160102 | 20160104 | 20160729 | 20160729 | PER | US-TEVA-623719USA | TEVA | 50.09 | YR | F | Y | 0.00000 | 20160729 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126053621 | 12605362 | 1 | PS | FLUCONAZOLE. | FLUCONAZOLE | 1 | N | 74681 | 150 | MG | TABLET |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126053621 | 12605362 | 1 | Vulvovaginal mycotic infection |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126053621 | 12605362 | Abdominal discomfort | |
126053621 | 12605362 | Abdominal distension | |
126053621 | 12605362 | Abdominal pain | |
126053621 | 12605362 | Abdominal pain upper | |
126053621 | 12605362 | Chills | |
126053621 | 12605362 | Decreased appetite | |
126053621 | 12605362 | Dizziness | |
126053621 | 12605362 | Flatulence | |
126053621 | 12605362 | Gastrointestinal pain | |
126053621 | 12605362 | Headache | |
126053621 | 12605362 | Nausea | |
126053621 | 12605362 | Pain |
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 |
---|---|---|---|---|---|---|
126053621 | 12605362 | 1 | 20160102 | 20160102 | 0 |