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
125381901 12538190 1 I 20160609 20160613 20160707 20160707 PER US-ACTELION-A-US2016-138168 ACTELION 51.00 YR A F Y 0.00000 20160707 MD 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
125381901 12538190 1 PS OPSUMIT MACITENTAN 1 Oral 10 MG, QD 204410 10 MG TABLET QD
125381901 12538190 2 SS ADCIRCA TADALAFIL 1 Oral 40 MG, UNK 0 40 MG
125381901 12538190 3 C ATORVASTATIN ATORVASTATIN 1 U 0
125381901 12538190 4 C RISPERDAL RISPERIDONE 1 U 0
125381901 12538190 5 C PRAVASTATIN. PRAVASTATIN 1 U 0
125381901 12538190 6 C CARVEDILOL. CARVEDILOL 1 U 0
125381901 12538190 7 C FUROSEMIDE. FUROSEMIDE 1 U 0
125381901 12538190 8 C KLOR-CON POTASSIUM CHLORIDE 1 U 0
125381901 12538190 9 C MONTELUKAST MONTELUKAST SODIUM 1 U 0
125381901 12538190 10 C TRAMADOL. TRAMADOL 1 U 0
125381901 12538190 11 C PREDNISONE. PREDNISONE 1 U 0
125381901 12538190 12 C LISINOPRIL. LISINOPRIL 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125381901 12538190 1 Product used for unknown indication
125381901 12538190 2 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125381901 12538190 Chest pain
125381901 12538190 Feeling abnormal

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
125381901 12538190 1 20160210 0
125381901 12538190 2 20160224 0