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
127770361 12777036 1 I 20070904 20160909 20160923 20160923 EXP US-AMNEAL PHARMACEUTICALS-2016AMN00598 AMNEAL 65.00 YR M Y 82.00000 KG 20160923 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
127770361 12777036 1 PS NAPROXEN. NAPROXEN 1 Oral UNK Y 75927
127770361 12777036 2 C NEXIUM ESOMEPRAZOLE MAGNESIUM 1 UNK Y 0
127770361 12777036 3 C DIOVAN HCT HYDROCHLOROTHIAZIDEVALSARTAN 1 UNK U 0
127770361 12777036 4 C ASA ASPIRIN 1 UNK 0
127770361 12777036 5 C PREVACID LANSOPRAZOLE 1 UNK 0
127770361 12777036 6 C AVODART DUTASTERIDE 1 UNK U 0
127770361 12777036 7 C METHOTREXATE. METHOTREXATE 1 UNK 0
127770361 12777036 8 C TRAMADOL. TRAMADOL 1 UNK U U 0
127770361 12777036 9 C MOBIC MELOXICAM 1 UNK 0
127770361 12777036 10 C FOLIC ACID. FOLIC ACID 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127770361 12777036 1 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
127770361 12777036 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127770361 12777036 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
127770361 12777036 1 20070824 20070904 0
127770361 12777036 2 20070824 20070904 0
127770361 12777036 4 2005 0
127770361 12777036 5 2002 0
127770361 12777036 6 200701 0
127770361 12777036 7 2001 0
127770361 12777036 8 2001 0
127770361 12777036 9 2001 0
127770361 12777036 10 2001 0