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
127752851 12775285 1 I 20090924 20160909 20160923 20160923 EXP US-AMNEAL PHARMACEUTICALS-2016AMN00603 AMNEAL 81.00 YR F Y 65.99000 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
127752851 12775285 1 PS NAPROXEN. NAPROXEN 1 UNK Y 75927
127752851 12775285 2 C SYNTHROID LEVOTHYROXINE SODIUM 1 UNK 0
127752851 12775285 3 C hydrochlorothiazide/lisinopril HYDROCHLOROTHIAZIDELISINOPRIL 1 UNK 0
127752851 12775285 4 C FOSAMAX ALENDRONATE SODIUM 1 UNK 0
127752851 12775285 5 C multivitamins with iron IRONVITAMINS 1 UNK 0
127752851 12775285 6 C NEXIUM ESOMEPRAZOLE MAGNESIUM 1 UNK Y 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127752851 12775285 1 Osteoarthritis

Outcome of event

Event ID CASEID OUTC COD
127752851 12775285 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127752851 12775285 Anaemia
127752851 12775285 Arrhythmia
127752851 12775285 Gastrointestinal haemorrhage

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
127752851 12775285 1 20080519 20090923 0
127752851 12775285 2 19950809 0
127752851 12775285 3 20020509 0
127752851 12775285 4 20000612 0
127752851 12775285 5 20080717 0
127752851 12775285 6 20080519 20090923 0