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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127408131 | 12740813 | 1 | I | 20151027 | 20160914 | 20160914 | PER | US-TEVA-605094USA | TEVA | 0.00 | F | Y | 0.00000 | 20160914 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127408131 | 12740813 | 1 | PS | FLUOXETINE | FLUOXETINE HYDROCHLORIDE | 1 | Unknown | Y | 6A404111 | 74803 | 20 | MG | CAPSULE |
Indications of drugs used
no results found |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127408131 | 12740813 | Anxiety | |
127408131 | 12740813 | Asthenia | |
127408131 | 12740813 | Balance disorder | |
127408131 | 12740813 | Feeling abnormal | |
127408131 | 12740813 | Headache | |
127408131 | 12740813 | Heart rate increased | |
127408131 | 12740813 | Nausea |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |