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
123941012 12394101 2 F 2010 20160729 20160523 20160808 EXP US-PFIZER INC-2016262572 PFIZER 75.00 YR F Y 0.00000 20160808 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
123941012 12394101 1 PS LIPITOR ATORVASTATIN CALCIUM 1 40 MG, 1X/DAY (ONCE DAILY) Y 20702 40 MG FILM-COATED TABLET QD
123941012 12394101 2 C ASPIRIN. ASPIRIN 1 81 MG, UNK 0 81 MG
123941012 12394101 3 C HYDRALAZINE HYDRALAZINE HYDROCHLORIDE 1 UNK 0
123941012 12394101 4 C LOSARTAN. LOSARTAN 1 UNK 0
123941012 12394101 5 C METOPROLOL. METOPROLOL 1 UNK 0
123941012 12394101 6 C CLONIDINE. CLONIDINE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123941012 12394101 1 Blood cholesterol abnormal

Outcome of event

Event ID CASEID OUTC COD
123941012 12394101 OT
123941012 12394101 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123941012 12394101 Muscular weakness
123941012 12394101 Polymyositis

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
123941012 12394101 1 2010 20140414 0