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
123673963 12367396 3 F 20160428 20160720 20160513 20160803 EXP CA-PFIZER INC-2016249336 PFIZER 59.00 YR F Y 0.00000 20160803 PH CA CA

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
123673963 12367396 1 PS REVATIO SILDENAFIL CITRATE 1 Oral 20 MG, 3X/DAY 21845 20 MG FILM-COATED TABLET TID
123673963 12367396 2 C BISOPROLOL BISOPROLOL 1 UNK 0
123673963 12367396 3 C PROFERRIN 2 UNK 0
123673963 12367396 4 C SPIRONOLACTONE. SPIRONOLACTONE 1 UNK 0
123673963 12367396 5 C SLOW K POTASSIUM CHLORIDE 1 UNK 0
123673963 12367396 6 C CARIPUL EPOPROSTENOL 1 UNK 0
123673963 12367396 7 C CALCIUM CALCIUM 1 UNK 0
123673963 12367396 8 C VITAMIN B12 CYANOCOBALAMIN 1 UNK 0
123673963 12367396 9 C VITAMIN D CHOLECALCIFEROL 1 UNK 0
123673963 12367396 10 C FUROSEMIDE. FUROSEMIDE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123673963 12367396 1 Pulmonary arterial hypertension

Outcome of event

Event ID CASEID OUTC COD
123673963 12367396 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123673963 12367396 Cough
123673963 12367396 Dyspnoea
123673963 12367396 Haemoptysis

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
123673963 12367396 1 20150227 0