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
125378441 12537844 1 I 20160131 20160623 20160707 20160707 EXP DE-TEVA-671498GER TEVA 1.00 DY F Y 3.25000 KG 20160707 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
125378441 12537844 1 PS CITALOPRAM CITALOPRAM HYDROBROMIDE 1 Transplacental IN THE BEGINNING 40 MG/D, IN WEEK 25 REDUCTION TO 20 MG/D 77232
125378441 12537844 2 SS RISPERDAL RISPERIDONE 1 Transplacental .5 MILLIGRAM DAILY; 0 .5 MG QD
125378441 12537844 3 C Elontril BUPROPION HYDROCHLORIDE 1 Transplacental DOSAGE UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125378441 12537844 1 Attention deficit/hyperactivity disorder
125378441 12537844 2 Attention deficit/hyperactivity disorder
125378441 12537844 3 Attention deficit/hyperactivity disorder

Outcome of event

Event ID CASEID OUTC COD
125378441 12537844 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125378441 12537844 Caput succedaneum
125378441 12537844 Foetal exposure during pregnancy
125378441 12537844 Hypotonia neonatal
125378441 12537844 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
125378441 12537844 1 20150508 20160131 0
125378441 12537844 2 20150508 20160131 0