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
127111671 12711167 1 I 20160714 20160826 20160902 20160902 EXP GB-MHRA-EYC 00144197 PHHY2016GB118047 SANDOZ 21.00 YR F Y 73.47000 KG 20160902 OT 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
127111671 12711167 1 PS CITALOPRAM CITALOPRAM HYDROBROMIDE 1 Oral 10MG (INCREASED TO 20MG FOR 2 DAYS) Y 8046068 77040
127111671 12711167 2 C PROPRANOLOL PROPRANOLOLPROPRANOLOL HYDROCHLORIDE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127111671 12711167 1 Depression
127111671 12711167 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127111671 12711167 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127111671 12711167 Anxiety
127111671 12711167 Migraine
127111671 12711167 Nausea
127111671 12711167 Self-injurious ideation
127111671 12711167 Suicidal ideation

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
127111671 12711167 1 20160714 20160815 0