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
126405611 12640561 1 I 20120801 20160804 20160810 20160810 EXP NO-PFIZER INC-2016375414 PFIZER 66.00 YR F Y 0.00000 20160810 LW NO NO

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
126405611 12640561 1 PS LIPITOR ATORVASTATIN CALCIUM 1 20 MG, UNK N 20702 20 MG
126405611 12640561 2 SS LIPITOR ATORVASTATIN CALCIUM 1 40 MG, UNK N 20702 40 MG
126405611 12640561 3 SS LIPITOR ATORVASTATIN CALCIUM 1 20 MG, UNK N 20702 20 MG
126405611 12640561 4 C METOPROLOL. METOPROLOL 1 UNK 0
126405611 12640561 5 C ALBYL-E ASPIRINMAGNESIUM OXIDE 1 UNK 0
126405611 12640561 6 C ATACAND CANDESARTAN CILEXETIL 1 UNK 0
126405611 12640561 7 C AMLODIPIN AMLODIPINE BESYLATE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126405611 12640561 1 Blood cholesterol increased

Outcome of event

Event ID CASEID OUTC COD
126405611 12640561 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
126405611 12640561 Balance disorder
126405611 12640561 Blood creatine phosphokinase increased
126405611 12640561 Blood creatinine increased
126405611 12640561 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
126405611 12640561 1 20120224 20120829 0
126405611 12640561 2 20120829 20120925 0
126405611 12640561 3 20120925 20121025 0