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
127093072 12709307 2 F 20151117 20160829 20160901 20160902 EXP GB-MHRA-ADR 23615525 PHFR2016GB007005 SANDOZ 60.00 YR Y 0.00000 20160902 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
127093072 12709307 1 I CARBAMAZEPINE. CARBAMAZEPINE 1 Unknown 1000 MG, 400 MG IN THE MORNING AND 600 MG AT NIGHT U 0 1000 MG
127093072 12709307 2 PS CLARITHROMYCIN. CLARITHROMYCIN 1 Unknown 500 MG, BID U 65136 500 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127093072 12709307 1 Epilepsy
127093072 12709307 2 Tooth abscess

Outcome of event

Event ID CASEID OUTC COD
127093072 12709307 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127093072 12709307 Diplopia
127093072 12709307 Disorientation
127093072 12709307 Dizziness
127093072 12709307 Dysarthria
127093072 12709307 Labelled drug-drug interaction medication error
127093072 12709307 Somnolence
127093072 12709307 Vertigo
127093072 12709307 Vision blurred

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

no results found

Therapies reported

no results found