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
125911992 12591199 2 F 201603 20160321 20160726 20160727 PER US-UNITED THERAPEUTICS-UNT-2016-004716 UNITED THERAPEUTICS 40.48 YR F Y 64.40000 KG 20160727 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
125911992 12591199 1 PS REMODULIN TREPROSTINIL 1 Intravenous drip 0.014 ?G/KG, CONTINUING U U 926618 21272 .014 UG/KG INJECTION
125911992 12591199 2 SS TYVASO TREPROSTINIL 1 18-54, MICROGRAMS, QID U U 2100747 0 INHALATION GAS QID
125911992 12591199 3 C OPSUMIT MACITENTAN 1 U U 0
125911992 12591199 4 C ADCIRCA TADALAFIL 1 U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125911992 12591199 1 Pulmonary hypertension
125911992 12591199 2 Product used for unknown indication
125911992 12591199 3 Product used for unknown indication
125911992 12591199 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125911992 12591199 Dermatitis contact
125911992 12591199 Injection site haemorrhage

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
125911992 12591199 1 20160203 0
125911992 12591199 2 20141112 0