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
127526541 12752654 1 I 20160718 20160909 20160916 20160916 EXP GB-ASTRAZENECA-2016SE96727 ASTRAZENECA 37.00 YR M Y 65.00000 KG 20160916 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
127526541 12752654 1 PS QUETIAPINE FUMARATE. QUETIAPINE FUMARATE 1 Oral 200.0MG UNKNOWN 20639 200 MG FILM-COATED TABLET
127526541 12752654 2 C BUSPIRONE BUSPIRONE HYDROCHLORIDE 1 0
127526541 12752654 3 C PAROXETINE. PAROXETINE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127526541 12752654 1 Generalised anxiety disorder

Outcome of event

Event ID CASEID OUTC COD
127526541 12752654 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127526541 12752654 Asthma
127526541 12752654 Eye irritation
127526541 12752654 Histamine level increased
127526541 12752654 Nasal congestion
127526541 12752654 Pruritus
127526541 12752654 Sneezing
127526541 12752654 Withdrawal syndrome

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
127526541 12752654 1 20141120 20160720 0