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
103036983 10303698 3 F 20160802 20140714 20160805 PER US-GILEAD-2013-0083605 GILEAD 43.00 YR A F Y 0.00000 20160805 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
103036983 10303698 1 PS AMBRISENTAN AMBRISENTAN 1 Unknown 10 MG, QD 1509427A 22081 10 MG TABLET QD
103036983 10303698 2 SS REMODULIN TREPROSTINIL 1 Unknown U U 0
103036983 10303698 3 C ADCIRCA TADALAFIL 1 U 0
103036983 10303698 4 C XARELTO RIVAROXABAN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
103036983 10303698 1 Product used for unknown indication
103036983 10303698 2 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
103036983 10303698 Device dislocation
103036983 10303698 Diarrhoea
103036983 10303698 Erythema
103036983 10303698 Pruritus

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found