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
127336491 12733649 1 I 20160905 20160912 20160912 EXP TR-TAKEDA-2016TUS016171 TAKEDA 0.00 N Y 0.00000 20160912 MD 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
127336491 12733649 1 PS COLCHICINE. COLCHICINE 1 Intra-uterine UNK 22352

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127336491 12733649 1 Foetal exposure timing unspecified

Outcome of event

Event ID CASEID OUTC COD
127336491 12733649 OT
127336491 12733649 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127336491 12733649 Intensive care
127336491 12733649 Premature baby

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

no results found

Therapies reported

no results found