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
123141204 12314120 4 F 20160706 20160428 20160721 PER US-ACTELION PHARMACEUTICALS US, INC.-A-US2016-135295 ACTELION 63.00 YR A F Y 0.00000 20160722 OT 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
123141204 12314120 1 PS VENTAVIS ILOPROST 1 Respiratory (inhalation) 5 MCG, 6 TO 9X/DAILY Y MA0299Z;MA02BP4 21779 5 UG INHALATION VAPOUR, SOLUTION
123141204 12314120 2 SS IRON IRON 1 Parenteral UNK U U 0
123141204 12314120 3 C ADCIRCA TADALAFIL 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123141204 12314120 1 Pulmonary arterial hypertension
123141204 12314120 2 Anaemia

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
123141204 12314120 Anaemia
123141204 12314120 Anxiety
123141204 12314120 Chest pain
123141204 12314120 Depression
123141204 12314120 Drug dose omission
123141204 12314120 Dysgeusia
123141204 12314120 Dyspnoea
123141204 12314120 Headache
123141204 12314120 Hypersomnia
123141204 12314120 Mineral supplementation
123141204 12314120 Myalgia
123141204 12314120 Nausea
123141204 12314120 Neck pain
123141204 12314120 Oedema peripheral

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
123141204 12314120 1 20151111 201606 0