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
127199831 12719983 1 I 20160628 20160826 20160907 20160907 EXP GB-MHRA-EYC 00144230 GB-DRREDDYS-GER/UKI/16/0082844 DR REDDYS 43.00 YR F Y 60.32000 KG 20160907 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
127199831 12719983 1 PS SERTRALINE SERTRALINE HYDROCHLORIDE 1 Oral Y U UNKNOWN 76442 100 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127199831 12719983 1 Depression

Outcome of event

Event ID CASEID OUTC COD
127199831 12719983 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127199831 12719983 Abnormal dreams
127199831 12719983 Anxiety
127199831 12719983 Blepharospasm
127199831 12719983 Bruxism
127199831 12719983 Decreased appetite
127199831 12719983 Depression
127199831 12719983 Diarrhoea
127199831 12719983 Dizziness
127199831 12719983 Essential tremor
127199831 12719983 Fatigue
127199831 12719983 Headache
127199831 12719983 Hot flush
127199831 12719983 Hypoglycaemia
127199831 12719983 Insomnia
127199831 12719983 Muscle twitching
127199831 12719983 Nausea

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
127199831 12719983 1 20160628 0