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
126783181 12678318 1 I 20160809 20160823 20160823 EXP GB-MHRA-EYC 00143337 GB-TEVA-684723ACC TEVA 41.00 YR F Y 58.96000 KG 20160823 CN GB GB

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
126783181 12678318 1 PS CITALOPRAM CITALOPRAM HYDROBROMIDE 1 Oral ALTERNATING WITH 7.5MG U U 77033 5 MG ORAL LIQUID
126783181 12678318 2 SS CITALOPRAM CITALOPRAM HYDROBROMIDE 1 Oral ALTERNATING WITH 5MG U U 77033 7.5 MG
126783181 12678318 3 SS CITALOPRAM CITALOPRAM HYDROBROMIDE 1 Oral EVERY OTHER DAY U U 77033 10 MG
126783181 12678318 4 SS CITALOPRAM CITALOPRAM HYDROBROMIDE 1 Oral U U 77033 20 MG
126783181 12678318 5 C ACTAVIS UK PREDNISOLONE 2 0
126783181 12678318 6 C GENERICS UK SULPHASALAZINE 2 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126783181 12678318 1 Anxiety

Outcome of event

Event ID CASEID OUTC COD
126783181 12678318 OT
126783181 12678318 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126783181 12678318 Blood pressure decreased
126783181 12678318 Heart rate abnormal
126783181 12678318 Palpitations
126783181 12678318 Syncope
126783181 12678318 Ventricular tachycardia

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
126783181 12678318 5 1997 0