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
127694311 12769431 1 I 20081022 20160908 20160921 20160921 EXP US-AMNEAL PHARMACEUTICALS-2016AMN00565 AMNEAL 74.00 YR M Y 0.00000 20160921 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
127694311 12769431 1 PS NAPROXEN. NAPROXEN 1 UNK Y 75927
127694311 12769431 2 C ALLOPURINOL. ALLOPURINOL 1 UNK 0
127694311 12769431 3 SS FUROSEMIDE. FUROSEMIDE 1 UNK 0
127694311 12769431 4 C COLCHICINE. COLCHICINE 1 UNK 0
127694311 12769431 5 C METOPROLOL. METOPROLOL 1 UNK 0
127694311 12769431 6 C LISINOPRIL. LISINOPRIL 1 UNK U 0
127694311 12769431 7 C PRAVASTATIN. PRAVASTATIN 1 UNK U 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
127694311 12769431 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127694311 12769431 Angina unstable
127694311 12769431 Cardiac failure congestive
127694311 12769431 Myocardial infarction

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
127694311 12769431 1 20080917 20081022 0
127694311 12769431 2 200802 0
127694311 12769431 3 1998 0
127694311 12769431 4 200802 0
127694311 12769431 5 200802 0
127694311 12769431 6 200802 0
127694311 12769431 7 2005 0