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
127085931 12708593 1 I 20131011 20131017 20160901 20160901 EXP US-PFIZER INC-2013297774 PFIZER 74.00 YR F Y 83.90000 KG 20160901 OT 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
127085931 12708593 1 PS IBUPROFEN. IBUPROFEN 1 Oral UNK 18989 TABLET
127085931 12708593 2 SS IBUPROFEN. IBUPROFEN 1 18989 TABLET
127085931 12708593 3 SS AMLODIPINE BESILATE AMLODIPINE BESYLATE 1 Oral 5 MG, DAILY Y 19787 5 MG
127085931 12708593 4 SS METOPROLOL TARTRATE. METOPROLOL TARTRATE 1 Oral 25 MG, 2X/DAY 2500 MG Y 74133 25 MG BID
127085931 12708593 5 SS METOPROLOL TARTRATE. METOPROLOL TARTRATE 1 Oral 12.5 MG, SINGLE 2500 MG Y 74133 12.5 MG
127085931 12708593 6 C NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Oral QD 0 QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127085931 12708593 1 Osteoarthritis
127085931 12708593 2 Rheumatoid arthritis
127085931 12708593 3 Hypertension
127085931 12708593 4 Coronary artery disease
127085931 12708593 6 Prophylaxis

Outcome of event

Event ID CASEID OUTC COD
127085931 12708593 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127085931 12708593 Orthostatic hypotension
127085931 12708593 Syncope

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
127085931 12708593 1 20120524 20130508 0
127085931 12708593 3 2004 20131011 0
127085931 12708593 4 20130823 20131011 0
127085931 12708593 5 20131013 20131013 0
127085931 12708593 6 20120524 20130508 0