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
125381922 12538192 2 F 20160803 20160707 20160815 EXP US-ACTELION-A-US2016-139008 ACTELION 41.00 YR A F Y 0.00000 20160815 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
125381922 12538192 1 PS UPTRAVI SELEXIPAG 1 Oral 200 MCG, BID U U 031004701 207947 200 UG TABLET BID
125381922 12538192 2 SS LETAIRIS AMBRISENTAN 1 Unknown 10 MG, UNK 0 10 MG QD
125381922 12538192 3 C ADCIRCA TADALAFIL 1 U 0
125381922 12538192 4 C XARELTO RIVAROXABAN 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125381922 12538192 1 Pulmonary hypertension
125381922 12538192 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125381922 12538192 HO
125381922 12538192 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125381922 12538192 Nausea
125381922 12538192 Retching
125381922 12538192 Systemic lupus erythematosus

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
125381922 12538192 1 20160414 0