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
126141801 12614180 1 I 2011 20160725 20160802 20160802 EXP US-PFIZER INC-2016361486 PFIZER 77.00 YR F Y 0.00000 20160802 MD 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
126141801 12614180 1 PS LIPITOR ATORVASTATIN CALCIUM 1 Oral 20 MG, DAILY 20702 20 MG FILM-COATED TABLET
126141801 12614180 2 SS LIPITOR ATORVASTATIN CALCIUM 1 20702 FILM-COATED TABLET
126141801 12614180 3 SS NORVASC AMLODIPINE BESYLATE 1 Oral 2.5 MG, 1X/DAY 19787 2.5 MG FILM-COATED TABLET QD
126141801 12614180 4 SS LEVOTHYROXINE SODIUM. LEVOTHYROXINE SODIUM 1 Oral 25 UG, DAILY 21301 25 UG TABLET
126141801 12614180 5 SS NIASPAN NIACIN 1 Oral 500 MG, DAILY 0 500 MG
126141801 12614180 6 SS ZETIA EZETIMIBE 1 10 MG, 1X/DAY 0 10 MG QD
126141801 12614180 7 SS ZETIA EZETIMIBE 1 0
126141801 12614180 8 C FOLIC ACID. FOLIC ACID 1 Oral 6 MG, DAILY (1 MILLIGRAM TABLET, 6 IN 1 DAY) 0 6 MG TABLET
126141801 12614180 9 C ASPIRIN. ASPIRIN 1 Oral 325 MG, DAILY 0 325 MG TABLET
126141801 12614180 10 C METHYLPREDNISOLONE. METHYLPREDNISOLONE 1 Oral 4 MG, UNK 0 4 MG TABLET
126141801 12614180 11 C NITROGLYCERINE NITROGLYCERIN 1 Sublingual 1 DF, AS NEEDED (0.4 MG/SPRAY,1 SPRAY) 0 1 DF
126141801 12614180 12 C NITROGLYCERINE NITROGLYCERIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126141801 12614180 1 Cardiac disorder
126141801 12614180 2 Hyperlipidaemia
126141801 12614180 3 Cardiac disorder
126141801 12614180 4 Thyroid disorder
126141801 12614180 5 Cardiac disorder
126141801 12614180 6 Cardiac disorder
126141801 12614180 7 Hyperlipidaemia
126141801 12614180 11 Chest pain
126141801 12614180 12 Coronary artery disease

Outcome of event

Event ID CASEID OUTC COD
126141801 12614180 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126141801 12614180 Hypoacusis

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
126141801 12614180 1 1999 0
126141801 12614180 3 20120404 0
126141801 12614180 4 20100503 0
126141801 12614180 5 2010 0
126141801 12614180 6 1999 0
126141801 12614180 8 20100428 0
126141801 12614180 9 20140728 0
126141801 12614180 10 20151008 0
126141801 12614180 11 20140117 0