The Safety Rates Drug Report

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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
125950401 12595040 1 I 201512 20160104 20160726 20160726 PER US-UNITED THERAPEUTICS-UNT-2016-000100 UNITED THERAPEUTICS 74.42 YR F Y 106.12000 KG 20160726 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
125950401 12595040 1 PS ORENITRAM TREPROSTINIL 1 Oral 1.375 MG, TID U U 2100397 203496 1.375 MG TABLET TID
125950401 12595040 2 SS ORENITRAM TREPROSTINIL 1 Oral UNK U U 2100684 203496 TABLET
125950401 12595040 3 SS LETAIRIS AMBRISENTAN 1 Unknown 10 MG, QD 1500226A 0 10 MG TABLET QD
125950401 12595040 4 SS REVATIO SILDENAFIL CITRATE 1 U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125950401 12595040 1 Pulmonary hypertension
125950401 12595040 3 Product used for unknown indication
125950401 12595040 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125950401 12595040 Pleural effusion
125950401 12595040 Pneumonia

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
125950401 12595040 1 20151007 0
125950401 12595040 3 20150508 0