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
126029331 12602933 1 I 20160106 20160728 20160728 EXP US-BAYER-2016-004664 BAYER 80.00 YR E F Y 90.70000 KG 20160728 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
126029331 12602933 1 PS ADEMPAS RIOCIGUAT 1 Oral 0.5 MG, TID BXH5601 204819 .5 MG TID
126029331 12602933 2 SS ADEMPAS RIOCIGUAT 1 Oral 2.5 MG, TID BXH7CK4 204819 2.5 MG TID
126029331 12602933 3 SS ADEMPAS RIOCIGUAT 1 Oral 2.5 MG, TID BXH8FC1 204819 2.5 MG TID
126029331 12602933 4 SS REGLAN METOCLOPRAMIDE HYDROCHLORIDE 1 UNK 0
126029331 12602933 5 C APIXABAN APIXABAN 1 UNK 0
126029331 12602933 6 C LETAIRIS AMBRISENTAN 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126029331 12602933 1 Pulmonary hypertension
126029331 12602933 2 Pulmonary hypertension
126029331 12602933 3 Pulmonary hypertension

Outcome of event

Event ID CASEID OUTC COD
126029331 12602933 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126029331 12602933 Abdominal distension
126029331 12602933 Blood glucose decreased
126029331 12602933 Coma
126029331 12602933 Contusion
126029331 12602933 Cough
126029331 12602933 Dyspnoea
126029331 12602933 Fall
126029331 12602933 Flatulence
126029331 12602933 Fluid retention
126029331 12602933 Hypotension
126029331 12602933 Somnolence
126029331 12602933 Unresponsive to stimuli

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
126029331 12602933 1 20151217 0