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
126337481 12633748 1 I 20160627 20160727 20160808 20160808 EXP CH-SM-2016-06200 CH-BAYER-2016-145966 BAYER 69.00 YR E F Y 0.00000 20160808 OT CH CH

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
126337481 12633748 1 PS ADEMPAS RIOCIGUAT 1 1 MG, UNK 204819 1 MG TABLET
126337481 12633748 2 SS NOVALGIN METAMIZOLE SODIUM 1 500 MG, 1 DOSE 20-JUN-2016 +/- 2 DAYSX1 DOSE 30-JUN-2016 Y 0 500 MG
126337481 12633748 3 SS NOVALGIN METAMIZOLE SODIUM 1 Y 0
126337481 12633748 4 SS OPSUMIT MACITENTAN 1 UNK 0
126337481 12633748 5 SS PANTOZOL PANTOPRAZOLE SODIUM 1 Oral SINCE AT LEAST 3 YEARS 0
126337481 12633748 6 SS IMUREK AZATHIOPRINE 1 Oral 50 MG, BID 0 50 MG BID
126337481 12633748 7 SS TORASEMIDE TORSEMIDE 1 Oral 15 MG, QD, SINCE LONGER TIME (}3 MONTHS) 0 15 MG QD
126337481 12633748 8 C REMODULIN TREPROSTINIL 1 Intravenous drip .0325 ?G/KG, Q1MIN CONTINUOUS INFUSION BY PUMP 0 .033 UG/KG /min
126337481 12633748 9 C REMODULIN TREPROSTINIL 1 0
126337481 12633748 10 C MARCOUMAR PHENPROCOUMON 1 PRN BY INR 0 3 MG
126337481 12633748 11 C SPIRICORT PREDNISOLONE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126337481 12633748 1 Pulmonary arterial hypertension
126337481 12633748 2 Rheumatic disorder
126337481 12633748 3 Arthralgia
126337481 12633748 4 Pulmonary arterial hypertension
126337481 12633748 6 Interstitial lung disease
126337481 12633748 8 Pulmonary arterial hypertension
126337481 12633748 9 Interstitial lung disease
126337481 12633748 11 Interstitial lung disease

Outcome of event

Event ID CASEID OUTC COD
126337481 12633748 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126337481 12633748 Agranulocytosis
126337481 12633748 Anaemia macrocytic
126337481 12633748 Thrombocytopenia

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
126337481 12633748 1 20160614 0
126337481 12633748 4 201408 0
126337481 12633748 6 201308 0