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
126935901 12693590 1 I 201607 20160719 20160829 20160829 EXP US-UNITED THERAPEUTICS-UNT-2016-011606 UNITED THERAPEUTICS 56.85 YR F Y 74.83000 KG 20160829 CN 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
126935901 12693590 1 PS REMODULIN TREPROSTINIL 1 Subcutaneous 0.036 ?G/KG, CONTINUING U U 2100701 21272 .036 UG/KG INJECTION
126935901 12693590 2 SS REVATIO SILDENAFIL CITRATE 1 Unknown U U 0
126935901 12693590 3 C VERAPAMIL VERAPAMIL HYDROCHLORIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126935901 12693590 1 Pulmonary arterial hypertension
126935901 12693590 2 Product used for unknown indication
126935901 12693590 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126935901 12693590 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126935901 12693590 Cough
126935901 12693590 Diarrhoea
126935901 12693590 Dyspnoea
126935901 12693590 Oxygen saturation decreased
126935901 12693590 Panic attack
126935901 12693590 Pulmonary congestion

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
126935901 12693590 1 20080722 0