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
127165851 12716585 1 I 20151117 20160829 20160906 20160906 EXP GB-ABBVIE-16P-167-1719456-00 ABBVIE 60.00 YR Y 0.00000 20160906 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
127165851 12716585 1 PS CLARITHROMYCIN. CLARITHROMYCIN 1 Unknown U UNKNOWN 50662 500 MG BID
127165851 12716585 2 I CARBAMAZEPINE. CARBAMAZEPINE 1 Unknown MODIFIED RELEASE 400MG IN THE MORNING AND 600MG AT NIGHT U UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127165851 12716585 1 Tooth abscess
127165851 12716585 2 Epilepsy

Outcome of event

Event ID CASEID OUTC COD
127165851 12716585 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127165851 12716585 Diplopia
127165851 12716585 Disorientation
127165851 12716585 Dizziness
127165851 12716585 Dysarthria
127165851 12716585 Labelled drug-drug interaction medication error
127165851 12716585 Somnolence
127165851 12716585 Vertigo
127165851 12716585 Vision blurred

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

no results found

Therapies reported

no results found