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
1143803618 11438036 18 F 2015 20160913 20150831 20160919 EXP DE-ACTELION-A-US2015-123316 ACTELION 54.00 YR A M Y 0.00000 20160919 OT DE KR

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
1143803618 11438036 1 PS VENTAVIS ILOPROST 1 Respiratory (inhalation) UNK 21779 INHALATION VAPOUR, SOLUTION
1143803618 11438036 2 SS VENTAVIS ILOPROST 1 Respiratory (inhalation) UNK 21779 INHALATION VAPOUR, SOLUTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
1143803618 11438036 1 Pulmonary arterial hypertension

Outcome of event

Event ID CASEID OUTC COD
1143803618 11438036 HO
1143803618 11438036 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
1143803618 11438036 Arrhythmia
1143803618 11438036 Ascites
1143803618 11438036 Blood test abnormal
1143803618 11438036 Chest discomfort
1143803618 11438036 Chest pain
1143803618 11438036 Cough
1143803618 11438036 Decreased appetite
1143803618 11438036 Dizziness
1143803618 11438036 Dry eye
1143803618 11438036 Dyspepsia
1143803618 11438036 Dyspnoea
1143803618 11438036 Eye pain
1143803618 11438036 Furuncle
1143803618 11438036 Heart rate increased
1143803618 11438036 Oedema peripheral
1143803618 11438036 Productive cough
1143803618 11438036 Pruritus
1143803618 11438036 Renal function test abnormal
1143803618 11438036 Renal impairment
1143803618 11438036 Sleep disorder
1143803618 11438036 Stress
1143803618 11438036 Swelling
1143803618 11438036 Visual acuity reduced
1143803618 11438036 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
1143803618 11438036 1 20150605 0
1143803618 11438036 2 20160419 0