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
127302081 12730208 1 I 201602 20160905 20160909 20160909 EXP CN-PFIZER INC-2016419366 PFIZER 7.00 DEC M Y 0.00000 20160909 CN CN CN

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
127302081 12730208 1 PS LIPITOR ATORVASTATIN CALCIUM 1 Oral 20 MG, 1X/DAY N 20702 20 MG FILM-COATED TABLET QD
127302081 12730208 2 SS LIPITOR ATORVASTATIN CALCIUM 1 Oral 10 MG, 1X/DAY N M23263 20702 10 MG FILM-COATED TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127302081 12730208 1 Hyperlipidaemia

Outcome of event

Event ID CASEID OUTC COD
127302081 12730208 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127302081 12730208 Muscle contractions involuntary
127302081 12730208 Muscle enzyme increased
127302081 12730208 Muscle spasms
127302081 12730208 Muscular weakness

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
127302081 12730208 1 2010 2013 0
127302081 12730208 2 2013 20160805 0