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
123578782 12357878 2 F 20160428 20160714 20160512 20160720 PER US-ELI_LILLY_AND_COMPANY-US201605003624 ELI LILLY AND CO 73.00 YR F Y 0.00000 20160720 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
123578782 12357878 1 PS ADCIRCA TADALAFIL 1 Unknown 20 MG, QD 21368 20 MG TABLET QD
123578782 12357878 2 SS AMBRISENTAN AMBRISENTAN 1 Unknown 5 MG, QD 1412805A 0 5 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123578782 12357878 1 Product used for unknown indication
123578782 12357878 2 Pulmonary hypertension

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
123578782 12357878 Fluid retention
123578782 12357878 Headache
123578782 12357878 Migraine
123578782 12357878 Nasal congestion
123578782 12357878 Nausea
123578782 12357878 Respiratory disorder
123578782 12357878 Seasonal allergy
123578782 12357878 Sinus disorder
123578782 12357878 Sinusitis
123578782 12357878 Vomiting

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
123578782 12357878 1 20160427 0
123578782 12357878 2 20160423 0