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
125895801 12589580 1 I 20160209 20160725 20160725 PER US-APOTEX-2016AP006664 APOTEX 0.00 M Y 83.91000 KG 20160725 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
125895801 12589580 1 PS ATORVASTATIN CALCIUM. ATORVASTATIN CALCIUM 1 Oral 1 DF DAILY Y 90548 1 DF TABLET
125895801 12589580 2 SS ATORVASTATIN CALCIUM. ATORVASTATIN CALCIUM 1 Oral 0.5 DF, DAILY Y 90548 .5 DF TABLET
125895801 12589580 3 SS BENAZEPRIL BENAZEPRIL HYDROCHLORIDE 1 Unknown 10 MG, QD Y 0 10 MG
125895801 12589580 4 C PLAVIX CLOPIDOGREL BISULFATE 1 Unknown 75 MG, QD Y 0 75 MG
125895801 12589580 5 C PLAVIX CLOPIDOGREL BISULFATE 1 Unknown UNK Y 0
125895801 12589580 6 C METOPROLOL. METOPROLOL 1 Unknown 50 MG, QD U 0 50 MG
125895801 12589580 7 C METOPROLOL. METOPROLOL 1 Unknown 25 MG, QD U 0 25 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125895801 12589580 1 Blood cholesterol
125895801 12589580 3 Product used for unknown indication
125895801 12589580 4 Product used for unknown indication
125895801 12589580 6 Blood pressure measurement

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125895801 12589580 Arthralgia
125895801 12589580 Dizziness
125895801 12589580 Muscular weakness
125895801 12589580 Myalgia

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
125895801 12589580 4 20150820 0