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
115265823 11526582 3 F 20150822 20160914 20150919 20160929 EXP US-AUROBINDO-AUR-APU-2015-08223 AUROBINDO 51.04 YR F Y 0.00000 20160929 CN US US

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
115265823 11526582 1 PS CITALOPRAM CITALOPRAM HYDROBROMIDE 1 UNK U 77031 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
115265823 11526582 1 Menopausal symptoms

Outcome of event

Event ID CASEID OUTC COD
115265823 11526582 HO
115265823 11526582 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
115265823 11526582 Asthenia
115265823 11526582 Blood creatine phosphokinase increased
115265823 11526582 Chest pain
115265823 11526582 Condition aggravated
115265823 11526582 Dizziness
115265823 11526582 Dyspnoea
115265823 11526582 Fatigue
115265823 11526582 Intentional product use issue
115265823 11526582 Myocarditis
115265823 11526582 Syncope
115265823 11526582 Wrong technique in product usage process

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
115265823 11526582 1 201409 0