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
126643912 12664391 2 F 2013 20160810 20160818 20160822 EXP BR-009507513-1608BRA007340 MERCK 0.00 E M Y 78.00000 KG 20160822 CN BR BR

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
126643912 12664391 1 PS VYTORIN EZETIMIBESIMVASTATIN 1 Oral 10-20 MG, QD 21687 TABLET QD
126643912 12664391 2 C OLMETEC OLMESARTAN MEDOXOMIL 1 Oral 1 TABLET, DAILY 0 1 DF TABLET QD
126643912 12664391 3 C SOMALGIN ASPIRINDIHYDROXYALUMINUM AMINOACETATE ANHYDROUSMAGNESIUM CARBONATE 1 UNK 0 TABLET
126643912 12664391 4 C DENYL (citalopram hydrobromide) 2 UNK 0
126643912 12664391 5 C BRILINTA TICAGRELOR 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126643912 12664391 1 Hypertension
126643912 12664391 2 Hypertension
126643912 12664391 3 Hypertension
126643912 12664391 4 Prophylaxis
126643912 12664391 5 Thrombosis prophylaxis

Outcome of event

Event ID CASEID OUTC COD
126643912 12664391 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126643912 12664391 Abdominal pain upper
126643912 12664391 Anaemia
126643912 12664391 Blood thyroid stimulating hormone
126643912 12664391 Glaucoma
126643912 12664391 Haematochezia
126643912 12664391 Haemorrhage
126643912 12664391 Product use issue

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
126643912 12664391 1 2012 0
126643912 12664391 2 2012 0
126643912 12664391 3 2015 0