The Safety Rates Drug Report

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Drug     Injury     Quarter    

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