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
126711491 12671149 1 I 20160809 20160822 20160822 EXP DE-DRREDDYS-GER/GER/16/0082320 DR REDDYS 0.00 N F Y 4.20000 KG 20160822 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
126711491 12671149 1 PS LEVETIRACETAM. LEVETIRACETAM 1 Transmammary UNKNOWN 76920 2000 MG BID
126711491 12671149 2 SS LEVETIRACETAM. LEVETIRACETAM 1 Transmammary UNKNOWN 76920 BID
126711491 12671149 3 SS LAMICTAL LAMOTRIGINE 1 Transmammary 0 50 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126711491 12671149 1 Epilepsy
126711491 12671149 3 Epilepsy

Outcome of event

Event ID CASEID OUTC COD
126711491 12671149 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126711491 12671149 Dehydration
126711491 12671149 Foetal exposure during pregnancy
126711491 12671149 Gastrooesophageal reflux disease
126711491 12671149 General physical health deterioration
126711491 12671149 Selective eating disorder
126711491 12671149 Urinary tract infection

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found