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
124689524 12468952 4 F 20160709 20160615 20160713 EXP US-GILEAD-2016-0219102 GILEAD 56.00 YR A F Y 0.00000 20160713 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
124689524 12468952 1 PS AMBRISENTAN AMBRISENTAN 1 Unknown 10 MG, QD 1504768A 22081 10 MG TABLET QD
124689524 12468952 2 SS REMODULIN TREPROSTINIL 1 Unknown U 0
124689524 12468952 3 C VELETRI EPOPROSTENOL 1 18.5NG/KG/MIN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124689524 12468952 1 Product used for unknown indication
124689524 12468952 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
124689524 12468952 HO
124689524 12468952 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124689524 12468952 Cardiac failure congestive
124689524 12468952 Diarrhoea
124689524 12468952 Dyspnoea
124689524 12468952 Fatigue
124689524 12468952 Fluid overload
124689524 12468952 Pain in jaw
124689524 12468952 Pulmonary arterial hypertension
124689524 12468952 Pulmonary embolism
124689524 12468952 Respiratory failure
124689524 12468952 Weight decreased

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

no results found

Therapies reported

no results found