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
121102522 12110252 2 F 20160215 20160627 20160224 20160701 EXP US-ACTELION-A-US2016-131692 ACTELION 73.00 YR E F Y 0.00000 20160701 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
121102522 12110252 1 PS VENTAVIS ILOPROST 1 Respiratory (inhalation) 5 MCG, 6X/DAY 21779 5 UG INHALATION VAPOUR, SOLUTION
121102522 12110252 2 SS VENTAVIS ILOPROST 1 Respiratory (inhalation) 5 MCG, QID 21779 5 UG INHALATION VAPOUR, SOLUTION QID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121102522 12110252 1 Pulmonary arterial hypertension

Outcome of event

Event ID CASEID OUTC COD
121102522 12110252 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
121102522 12110252 Anaemia
121102522 12110252 Asthenia
121102522 12110252 Dizziness
121102522 12110252 Dyspnoea
121102522 12110252 Fall
121102522 12110252 Gastric ulcer
121102522 12110252 Haemoglobin decreased
121102522 12110252 Red blood cell count decreased
121102522 12110252 Transfusion

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
121102522 12110252 1 20151218 0