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
127741061 12774106 1 I 20160718 20160909 20160923 20160923 EXP GB-MHRA-EYC 00144814 GB-LUPIN PHARMACEUTICALS INC.-E2B_00006171 LUPIN 37.00 YR M Y 65.00000 KG 20160923 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
127741061 12774106 1 PS QUETIAPINE FUMARATE. QUETIAPINE FUMARATE 1 Oral D U UNKNOWN 201109 200 MG
127741061 12774106 2 SS QUETIAPINE FUMARATE. QUETIAPINE FUMARATE 1 Oral D U UNKNOWN 201109
127741061 12774106 3 C BUSPIRONE BUSPIRONE HYDROCHLORIDE 1 Unknown 0
127741061 12774106 4 C PAROXETINE. PAROXETINE 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127741061 12774106 1 Generalised anxiety disorder
127741061 12774106 3 Product used for unknown indication
127741061 12774106 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127741061 12774106 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127741061 12774106 Asthma
127741061 12774106 Eye irritation
127741061 12774106 Histamine level increased
127741061 12774106 Nasal congestion
127741061 12774106 Pruritus
127741061 12774106 Sneezing
127741061 12774106 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
127741061 12774106 1 20141120 0
127741061 12774106 2 20160720 0