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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127577651 | 12757765 | 1 | I | 20160811 | 20160907 | 20160919 | 20160919 | EXP | DE-SUN PHARMACEUTICAL INDUSTRIES LTD-2016R1-123874 | RANBAXY | 1.00 | DY | M | Y | 2.21000 | KG | 20160919 | OT | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127577651 | 12757765 | 1 | PS | DULOXETINE. | DULOXETINE | 1 | Transplacental | 30 MG, QD | U | 90745 | 30 | MG | |||||||
127577651 | 12757765 | 2 | SS | RISPERIDONE. | RISPERIDONE | 1 | Transplacental | 3[MG/D(-2)] | U | 0 | |||||||||
127577651 | 12757765 | 3 | SS | AKINETON | BIPERIDEN HYDROCHLORIDE | 1 | Transplacental | UNK | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127577651 | 12757765 | 1 | Bipolar disorder |
127577651 | 12757765 | 2 | Bipolar disorder |
127577651 | 12757765 | 3 | Extrapyramidal disorder |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127577651 | 12757765 | OT |
127577651 | 12757765 | CA |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127577651 | 12757765 | Foetal exposure during pregnancy | |
127577651 | 12757765 | Gastroschisis | |
127577651 | 12757765 | Premature baby |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |