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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
99585012 | 9958501 | 2 | F | 20130728 | 20160915 | 20140305 | 20160921 | EXP | GB-DRREDDYS-GER/UKI/14/0038593 | DR REDDYS | 0.00 | DY | M | Y | 3.99000 | KG | 20160921 | CN | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
99585012 | 9958501 | 1 | PS | QUETIAPINE. | QUETIAPINE | 1 | Transplacental | D | UNKNOWN | 77380 | 200 | MG | QD | ||||||
99585012 | 9958501 | 2 | SS | ARIPIPRAZOLE. | ARIPIPRAZOLE | 1 | Transplacental | D | 0 | 10 | MG | ||||||||
99585012 | 9958501 | 3 | SS | DULOXETINE HYDROCHLORIDE. | DULOXETINE HYDROCHLORIDE | 1 | Transplacental | D | 0 | 60 | MG | QD | |||||||
99585012 | 9958501 | 4 | SS | Zopiclone | ZOPICLONE | 1 | Transplacental | D | 0 | 7.5 | MG | QD | |||||||
99585012 | 9958501 | 5 | SS | ZYPREXA | OLANZAPINE | 1 | Transplacental | D | 0 | 10 | MG | QD | |||||||
99585012 | 9958501 | 6 | SS | ZYPREXA | OLANZAPINE | 1 | Transplacental | D | 0 | 15 | MG | QD | |||||||
99585012 | 9958501 | 7 | SS | ZYPREXA | OLANZAPINE | 1 | Transmammary | D | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
99585012 | 9958501 | 1 | Product used for unknown indication |
99585012 | 9958501 | 2 | Product used for unknown indication |
99585012 | 9958501 | 3 | Product used for unknown indication |
99585012 | 9958501 | 4 | Product used for unknown indication |
99585012 | 9958501 | 5 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
99585012 | 9958501 | OT |
99585012 | 9958501 | CA |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
99585012 | 9958501 | Cleft palate | |
99585012 | 9958501 | Exposure during breast feeding | |
99585012 | 9958501 | Foetal exposure during pregnancy | |
99585012 | 9958501 | High arched palate | |
99585012 | 9958501 | Selective eating disorder |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |