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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125784001 | 12578400 | 1 | I | 2013 | 20160707 | 20160721 | 20160721 | EXP | DE-AUROBINDO-AUR-APL-2016-09628 | AUROBINDO | 21.00 | YR | F | Y | 78.00000 | KG | 20160721 | MD | DE | DE |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125784001 | 12578400 | 1 | PS | SERTRALINE | SERTRALINE HYDROCHLORIDE | 1 | Oral | Y | U | 77206 | |||||||||
125784001 | 12578400 | 2 | SS | Venlafaxine 75mg | VENLAFAXINE HYDROCHLORIDE | 1 | Oral | 75 MG, UNK | Y | U | 0 | 75 | MG |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125784001 | 12578400 | 1 | Depression |
125784001 | 12578400 | 2 | Depression |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125784001 | 12578400 | DS |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125784001 | 12578400 | Hepatic enzyme increased | |
125784001 | 12578400 | Intentional self-injury | |
125784001 | 12578400 | Sedation | |
125784001 | 12578400 | Weight increased |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |