The Safety Rates Drug Report

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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
125816001 12581600 1 I 20160714 20160722 20160722 PER US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-058809 BRISTOL MYERS SQUIBB 0.00 F Y 0.00000 20160721 CN 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
125816001 12581600 1 PS PRAVASTATIN SODIUM. PRAVASTATIN SODIUM 1 Unknown U 19898 TABLET
125816001 12581600 2 C NITROSTAT NITROGLYCERIN 1 Unknown 0.4 G, UNK U 0 .4 G
125816001 12581600 3 C TESSALON BENZONATATE 1 Unknown U 0
125816001 12581600 4 C NORVASC AMLODIPINE BESYLATE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125816001 12581600 1 Product used for unknown indication
125816001 12581600 2 Product used for unknown indication
125816001 12581600 3 Product used for unknown indication
125816001 12581600 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125816001 12581600 Hypersensitivity
125816001 12581600 Myalgia

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

no results found

Therapies reported

no results found