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
104147762 10414776 2 F 20140604 20140613 20140828 20160907 EXP TR-UNITED THERAPEUTICS-UNT-2014-002948 UNITED THERAPEUTICS 36.00 YR F Y 0.00000 20160907 MD TR TR

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
104147762 10414776 1 PS REMODULIN TREPROSTINIL 1 Subcutaneous 0.00025 ?G/KG, UNK Y U 21272 INJECTION
104147762 10414776 2 C BOSENTAN. BOSENTAN 1 U 0
104147762 10414776 3 C SILDENAFIL. SILDENAFIL 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
104147762 10414776 1 Pulmonary arterial hypertension
104147762 10414776 2 Product used for unknown indication
104147762 10414776 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
104147762 10414776 OT
104147762 10414776 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
104147762 10414776 Acute respiratory distress syndrome
104147762 10414776 Cyanosis
104147762 10414776 Dyspnoea
104147762 10414776 Exercise tolerance decreased
104147762 10414776 Pulmonary oedema
104147762 10414776 Pulmonary veno-occlusive disease
104147762 10414776 Rales
104147762 10414776 Syncope
104147762 10414776 Tachycardia

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
104147762 10414776 1 20140530 0