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
127403151 12740315 1 I 20160907 20160913 20160913 EXP US-AMNEAL PHARMACEUTICALS-2016AMN00508 AMNEAL 66.00 YR F Y 95.69000 KG 20160913 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
127403151 12740315 1 PS NAPROXEN. NAPROXEN 1 UNK Y 75927 TABLET
127403151 12740315 2 C ASPIRIN. ASPIRIN 1 UNK 0
127403151 12740315 3 C PLAVIX CLOPIDOGREL BISULFATE 1 UNK 0
127403151 12740315 4 C ATENOLOL. ATENOLOL 1 UNK 0
127403151 12740315 5 C DIOVAN VALSARTAN 1 UNK 0
127403151 12740315 6 C GLUCOPHAGE METFORMIN HYDROCHLORIDE 1 UNK 0
127403151 12740315 7 C GLIPIZIDE. GLIPIZIDE 1 UNK 0
127403151 12740315 8 C ZETIA EZETIMIBE 1 UNK 0
127403151 12740315 9 C NIASPAN NIACIN 1 UNK 0
127403151 12740315 10 C CALTRATE CALCIUM CARBONATE 1 UNK 0
127403151 12740315 11 C NITROGLYCERIN. NITROGLYCERIN 1 UNK 0

Indications of drugs used

no results found

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127403151 12740315 Coronary artery disease

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
127403151 12740315 1 20070405 20070508 0
127403151 12740315 2 20041228 0
127403151 12740315 3 20041228 0
127403151 12740315 4 20041228 0
127403151 12740315 5 1997 0
127403151 12740315 6 1999 0
127403151 12740315 7 1999 0
127403151 12740315 8 20050420 0
127403151 12740315 9 20050420 0
127403151 12740315 10 2004 0
127403151 12740315 11 2005 0