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
125227711 12522771 1 I 20160610 20160621 20160701 20160701 EXP NL-LRB-220939 NL-FRI-1000085834 FOREST 0.00 DY F Y 2.57000 KG 20160701 OT DK NL

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
125227711 12522771 1 PS ESCITALOPRAM ESCITALOPRAM OXALATE 1 Transplacental 21323 TABLET QD
125227711 12522771 2 C OMEPRAZOL CAPSULE MSR 40MG OMEPRAZOLE 1 Transplacental 40 MG 0 40 MG CAPSULE QD
125227711 12522771 3 C FOLIC ACID. FOLIC ACID 1 Transplacental 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125227711 12522771 1 Anxiety
125227711 12522771 2 Product used for unknown indication
125227711 12522771 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125227711 12522771 HO
125227711 12522771 CA

Reactions reported

Event ID CASEID DRUG REC ACT PT
125227711 12522771 Choanal atresia
125227711 12522771 Foetal exposure during pregnancy

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
125227711 12522771 1 2012 0