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
71849564 7184956 4 F 20090924 20160824 20091123 20160901 EXP US-PFIZER INC-2009295842 PFIZER 81.00 YR F Y 66.00000 KG 20160901 MD 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
71849564 7184956 1 PS NAPROXEN. NAPROXEN 1 Oral UNK Y 0 TABLET
71849564 7184956 2 C NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Oral 20 OR 40 MG, 1X/DAY 9860 MG 0 20 MG CAPSULE QD
71849564 7184956 3 C SYNTHROID LEVOTHYROXINE SODIUM 1 Oral 0.1 MG, 1X/DAY 0 .1 MG QD
71849564 7184956 4 C HYDROCHLOROTHIAZIDE/LISINOPRIL 2 Oral 10/12.5 MG 0
71849564 7184956 5 C FOSAMAX ALENDRONATE SODIUM 1 Oral UNK 0
71849564 7184956 6 C MULTIVITAMINS WITH IRON IRONVITAMINS 1 Oral UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
71849564 7184956 1 Osteoarthritis
71849564 7184956 3 Hypothyroidism
71849564 7184956 4 Hypertension
71849564 7184956 6 Anaemia

Outcome of event

Event ID CASEID OUTC COD
71849564 7184956 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
71849564 7184956 Anaemia
71849564 7184956 Arrhythmia
71849564 7184956 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
71849564 7184956 1 20080519 20090923 0
71849564 7184956 2 20080519 20090923 0
71849564 7184956 3 19950809 0
71849564 7184956 4 20020509 0
71849564 7184956 5 20000612 0
71849564 7184956 6 20080717 0