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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127393241 | 12739324 | 1 | I | 20160818 | 20160905 | 20160913 | 20160913 | EXP | GB-MHRA-EYC 00144566 | PHHY2016GB122452 | SANDOZ | 44.00 | YR | F | Y | 60.00000 | KG | 20160913 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127393241 | 12739324 | 1 | PS | SERTRALINE | SERTRALINE HYDROCHLORIDE | 1 | Oral | 50 MG, QD | 50 | MG | Y | U | 2768646 | 77713 | 50 | MG | QD | ||
127393241 | 12739324 | 2 | C | TRIMETHOPRIM. | TRIMETHOPRIM | 1 | Unknown | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127393241 | 12739324 | 1 | Anxiety |
127393241 | 12739324 | 2 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127393241 | 12739324 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127393241 | 12739324 | Diarrhoea | |
127393241 | 12739324 | Hepatic pain | |
127393241 | 12739324 | Insomnia | |
127393241 | 12739324 | Nausea | |
127393241 | 12739324 | Vertigo | |
127393241 | 12739324 | Vomiting |
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 |
---|---|---|---|---|---|---|
127393241 | 12739324 | 1 | 20160818 | 20160819 | 0 |