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
126462791 12646279 1 I 20160802 20160812 20160812 EXP TR-009507513-1608TUR005013 MERCK 0.00 Y 0.00000 20160812 OT TR TR

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
126462791 12646279 1 PS MIRTAZAPINE. MIRTAZAPINE 1 Transplacental UNK U 20415 TABLET
126462791 12646279 2 SS ESCITALOPRAM ESCITALOPRAM OXALATE 1 Transplacental UNK U 0
126462791 12646279 3 SS BUTYLSCOPOLAMINE BROMIDE BUTYLSCOPOLAMINE BROMIDE 1 Transplacental UNK U 0
126462791 12646279 4 SS MEDAZEPAM MEDAZEPAM 1 Transplacental UNK U 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126462791 12646279 CA
126462791 12646279 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126462791 12646279 Foetal exposure during pregnancy
126462791 12646279 Limb reduction defect

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

no results found

Therapies reported

no results found