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
125264141 12526414 1 I 20160131 20160623 20160705 20160705 EXP DE-DRREDDYS-GER/GER/16/0080983 DR REDDYS 1.00 DY F Y 3.25000 KG 20160705 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
125264141 12526414 1 PS CITALOPRAM CITALOPRAM HYDROBROMIDE 1 Transplacental 40 (MG/D) IN THE BEGINNING,IN WEEK 25 REDUCTION TO 20MG/D. UNKNOWN 77038
125264141 12526414 2 SS RISPERDAL RISPERIDONE 1 Transplacental 0 .5 MG/M**2 QD
125264141 12526414 3 C Elontril BUPROPION HYDROCHLORIDE 1 Transplacental 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125264141 12526414 1 Attention deficit/hyperactivity disorder
125264141 12526414 2 Attention deficit/hyperactivity disorder
125264141 12526414 3 Attention deficit/hyperactivity disorder

Outcome of event

Event ID CASEID OUTC COD
125264141 12526414 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125264141 12526414 Caput succedaneum
125264141 12526414 Foetal exposure during pregnancy
125264141 12526414 Hypotonia neonatal
125264141 12526414 Respiratory disorder neonatal

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
125264141 12526414 1 20150508 20160131 0
125264141 12526414 2 20150508 20160131 0