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
126804051 12680405 1 I 2008 20160819 20160824 20160824 EXP US-GLAXOSMITHKLINE-US2016121429 GLAXOSMITHKLINE 62.65 YR F Y 0.00000 20160824 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
126804051 12680405 1 PS VENTOLIN HFA ALBUTEROL SULFATE 1 2 PUFF(S), QID 20983 2 DF QID
126804051 12680405 2 C ASPIRIN. ASPIRIN 1 U 0
126804051 12680405 3 C ATORVASTATIN ATORVASTATIN 1 U 0
126804051 12680405 4 C CARVEDILOL. CARVEDILOL 1 U 0
126804051 12680405 5 C EFFIENT PRASUGREL HYDROCHLORIDE 1 U 0
126804051 12680405 6 C HYDROCODONE HYDROCODONE 1 U 0
126804051 12680405 7 C LOSARTAN. LOSARTAN 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126804051 12680405 1 Dyspnoea

Outcome of event

Event ID CASEID OUTC COD
126804051 12680405 HO
126804051 12680405 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126804051 12680405 Arthropathy
126804051 12680405 Blood cholesterol increased
126804051 12680405 Calcinosis
126804051 12680405 Cataract
126804051 12680405 Coronary arterial stent insertion
126804051 12680405 Device use error
126804051 12680405 Fall
126804051 12680405 Hypertension
126804051 12680405 Knee operation
126804051 12680405 Myocardial infarction
126804051 12680405 Pain
126804051 12680405 Upper limb fracture

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
126804051 12680405 1 2007 0