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
124207112 12420711 2 F 2016 20160629 20160531 20160712 EXP US-JUBILANT CADISTA PHARMACEUTICALS-2016JUB00188 JUBILANT 56.82 YR F Y 79.37000 KG 20160712 CN COUNTRY NOT SPECIFIED 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
124207112 12420711 1 PS PREDNISONE. PREDNISONE 1 U 40362
124207112 12420711 2 SS ORENITRAM TREPROSTINIL 1 Oral 0.25 MG, 3X/DAY 2100679 0 .25 MG TABLET TID
124207112 12420711 3 SS SILDENAFIL. SILDENAFIL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124207112 12420711 2 Pulmonary arterial hypertension

Outcome of event

Event ID CASEID OUTC COD
124207112 12420711 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124207112 12420711 Arthralgia
124207112 12420711 Chest pain
124207112 12420711 Diarrhoea
124207112 12420711 Dyspnoea
124207112 12420711 Hypertension
124207112 12420711 Pain in jaw
124207112 12420711 Temporomandibular joint syndrome
124207112 12420711 Throat tightness
124207112 12420711 Tooth disorder
124207112 12420711 Vomiting

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
124207112 12420711 2 20150520 0