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
125850731 12585073 1 I 201507 20160715 20160723 20160723 PER US-009507513-1607USA008600 MERCK 91.00 YR F Y 0.00000 20160723 MD US US

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
125850731 12585073 1 PS ZETIA EZETIMIBE 1 Oral UNK U 21445 TABLET
125850731 12585073 2 SS ZETIA EZETIMIBE 1 Oral UNK U 21445 TABLET
125850731 12585073 3 C AZOPT BRINZOLAMIDE 1 0
125850731 12585073 4 C LATANOPROST. LATANOPROST 1 0
125850731 12585073 5 C LIPROX 2 0
125850731 12585073 6 C CLARITIN LORATADINE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125850731 12585073 1 Blood cholesterol increased
125850731 12585073 3 Glaucoma
125850731 12585073 4 Eye disorder
125850731 12585073 5 Irritable bowel syndrome
125850731 12585073 6 Hypersensitivity

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125850731 12585073 Drug dose omission
125850731 12585073 Wrist fracture

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

no results found

Therapies reported

no results found