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
126032501 12603250 1 I 2016 20160721 20160728 20160728 EXP DE-ACTELION-A-NJ2016-140023 ACTELION 66.00 YR E M Y 0.00000 20160728 OT DE FR

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
126032501 12603250 1 PS VENTAVIS ILOPROST 1 Respiratory (inhalation) 9ID 21779 INHALATION VAPOUR, SOLUTION
126032501 12603250 2 SS VENTAVIS ILOPROST 1 Respiratory (inhalation) 6ID 21779 INHALATION VAPOUR, SOLUTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126032501 12603250 1 Pulmonary arterial hypertension

Outcome of event

Event ID CASEID OUTC COD
126032501 12603250 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126032501 12603250 Coma
126032501 12603250 Conjunctivitis
126032501 12603250 Dysuria
126032501 12603250 Headache
126032501 12603250 Ocular hyperaemia
126032501 12603250 Oral discomfort
126032501 12603250 Paraesthesia oral
126032501 12603250 Subdural haematoma
126032501 12603250 Tongue haemorrhage
126032501 12603250 Tongue injury
126032501 12603250 Tongue ulceration

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

no results found

Therapies reported

no results found