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
127291731 12729173 1 I 20151117 20160829 20160909 20160909 EXP GB-MHRA-ADR 23615525 GB-TEVA-689328ACC TEVA 60.00 YR Y 0.00000 20160909 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
127291731 12729173 1 PS CLARITHROMYCIN. CLARITHROMYCIN 1 1000 MILLIGRAM DAILY; U U 65155 500 MG BID
127291731 12729173 2 I CARBAMAZEPINE. CARBAMAZEPINE 1 MODIFIED RELEASE 400MG IN THE MORNING AND 600MG AT NIGHT. U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127291731 12729173 1 Tooth abscess
127291731 12729173 2 Epilepsy

Outcome of event

Event ID CASEID OUTC COD
127291731 12729173 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127291731 12729173 Diplopia
127291731 12729173 Disorientation
127291731 12729173 Dizziness
127291731 12729173 Dysarthria
127291731 12729173 Labelled drug-drug interaction medication error
127291731 12729173 Somnolence
127291731 12729173 Vertigo
127291731 12729173 Vision blurred

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found