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
109237683 10923768 3 F 20111220 20160919 20150318 20160921 EXP US-009507513-1503USA007144 MERCK 62.00 YR M Y 106.60000 KG 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
109237683 10923768 1 PS COZAAR LOSARTAN POTASSIUM 1 Oral 100 MG, QD 200 MG Y 20386 100 MG TABLET QD
109237683 10923768 2 SS IBUPROFEN. IBUPROFEN 1 Oral UNK D 0 TABLET
109237683 10923768 3 SS IBUPROFEN. IBUPROFEN 1 D 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
109237683 10923768 1 Hypertension
109237683 10923768 2 Rheumatoid arthritis
109237683 10923768 3 Osteoarthritis

Outcome of event

Event ID CASEID OUTC COD
109237683 10923768 OT
109237683 10923768 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
109237683 10923768 Acute kidney injury
109237683 10923768 Chest pain

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
109237683 10923768 1 20111219 20111220 0
109237683 10923768 2 20090130 20110603 0