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
125876442 12587644 2 F 20160729 20160725 20160803 EXP US-GILEAD-2016-0224648 GILEAD 77.00 YR E M Y 0.00000 20160803 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
125876442 12587644 1 PS AMBRISENTAN AMBRISENTAN 1 Unknown 10 MG, QD 1509427A 22081 10 MG TABLET QD
125876442 12587644 2 SS ADCIRCA TADALAFIL 1 Unknown U 0
125876442 12587644 3 SS PRIMIDONE. PRIMIDONE 1 Unknown U 0
125876442 12587644 4 C ADEMPAS RIOCIGUAT 1 0
125876442 12587644 5 C TYVASO TREPROSTINIL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125876442 12587644 1 Product used for unknown indication
125876442 12587644 2 Product used for unknown indication
125876442 12587644 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125876442 12587644 OT
125876442 12587644 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125876442 12587644 Cyanosis
125876442 12587644 Dyspnoea
125876442 12587644 Oxygen saturation decreased
125876442 12587644 Pulmonary arterial hypertension
125876442 12587644 Rash

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

no results found

Therapies reported

no results found