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
127261872 12726187 2 F 201607 20160905 20160908 20160914 EXP IT-MINISAL02-372981 IT-MYLANLABS-2016M1037697 MYLAN 0.00 Y 0.00000 20160914 MD IT IT

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
127261872 12726187 1 PS ATORVASTATIN ATORVASTATIN 1 Oral 10 MG, QD U U 91226 10 MG TABLET QD
127261872 12726187 2 SS PLAVIX CLOPIDOGREL BISULFATE 1 Oral DAILY U U 0 FILM-COATED TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127261872 12726187 1 Hypercholesterolaemia
127261872 12726187 2 Peripheral artery angioplasty

Outcome of event

Event ID CASEID OUTC COD
127261872 12726187 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127261872 12726187 Blood creatine phosphokinase increased
127261872 12726187 Pain in extremity

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

no results found

Therapies reported

no results found