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
126375453 12637545 3 F 201606 20160829 20160809 20160902 EXP US-ACTELION-A-NJ2016-138256 ACTELION 72.00 YR E F Y 0.00000 20160902 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
126375453 12637545 1 PS VENTAVIS ILOPROST 1 Respiratory (inhalation) 5 MCG, 6-9XDAY N MA02BP4 21779 5 UG INHALATION VAPOUR, SOLUTION
126375453 12637545 2 SS VENTAVIS ILOPROST 1 Respiratory (inhalation) 5 MCG, 6-8 X/DAY N MA02DL0 21779 5 UG INHALATION VAPOUR, SOLUTION
126375453 12637545 3 SS VENTAVIS ILOPROST 1 Respiratory (inhalation) UNK, 5 X/DAY N 21779 INHALATION VAPOUR, SOLUTION
126375453 12637545 4 SS UPTRAVI SELEXIPAG 1 Oral 200 MCG, BID N 031004701 207947 200 UG TABLET BID
126375453 12637545 5 SS UPTRAVI SELEXIPAG 1 Oral 400 MCG, BID N 031004701 207947 400 UG TABLET BID
126375453 12637545 6 C ADCIRCA TADALAFIL 1 U 0
126375453 12637545 7 C NIFEDIPINE. NIFEDIPINE 1 U 0
126375453 12637545 8 C COUMADIN WARFARIN SODIUM 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126375453 12637545 1 Pulmonary arterial hypertension
126375453 12637545 4 Pulmonary arterial hypertension

Outcome of event

Event ID CASEID OUTC COD
126375453 12637545 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126375453 12637545 Blood pressure fluctuation
126375453 12637545 Cataract operation
126375453 12637545 Cellulitis
126375453 12637545 Contusion
126375453 12637545 Dizziness
126375453 12637545 Eye irritation
126375453 12637545 Fall
126375453 12637545 Headache
126375453 12637545 Insomnia
126375453 12637545 Joint injury
126375453 12637545 Limb injury
126375453 12637545 Loss of consciousness
126375453 12637545 Oxygen saturation decreased
126375453 12637545 Pain
126375453 12637545 Peripheral swelling
126375453 12637545 Sudden onset of sleep
126375453 12637545 Weight increased

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
126375453 12637545 1 20130718 0
126375453 12637545 4 20160518 0