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
91478264 9147826 4 F 20160721 20130307 20160729 EXP US-ELI_LILLY_AND_COMPANY-US201302010410 ELI LILLY AND CO 0.00 F Y 0.00000 20160728 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
91478264 9147826 1 PS ADCIRCA TADALAFIL 1 Oral 40 MG, QD U 21368 40 MG QD
91478264 9147826 2 C LETAIRIS AMBRISENTAN 1 U 0
91478264 9147826 3 C VESICARE SOLIFENACIN SUCCINATE 1 U 0
91478264 9147826 4 C NORVASC AMLODIPINE BESYLATE 1 U 0
91478264 9147826 5 C LEVOTHYROXINE. LEVOTHYROXINE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
91478264 9147826 1 Pulmonary hypertension

Outcome of event

Event ID CASEID OUTC COD
91478264 9147826 HO
91478264 9147826 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
91478264 9147826 Diarrhoea
91478264 9147826 Disease progression
91478264 9147826 Gait disturbance
91478264 9147826 Gastrointestinal sounds abnormal
91478264 9147826 Headache
91478264 9147826 Hepatomegaly
91478264 9147826 Ileus
91478264 9147826 Malaise
91478264 9147826 Muscular weakness
91478264 9147826 Myalgia
91478264 9147826 Nasal congestion
91478264 9147826 Nausea
91478264 9147826 Pain
91478264 9147826 Splenomegaly
91478264 9147826 Thrombosis
91478264 9147826 Weight decreased

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
91478264 9147826 1 20120917 2014 0