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
127668962 12766896 2 F 20160922 20160922 20160921 20160928 EXP CA-PFIZER INC-2016437837 PFIZER 52.00 YR F Y 0.00000 20160928 CN 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
127668962 12766896 1 PS REVATIO SILDENAFIL CITRATE 1 Oral UNK U 21845 FILM-COATED TABLET
127668962 12766896 2 SS REVATIO SILDENAFIL CITRATE 1 U 21845 FILM-COATED TABLET
127668962 12766896 3 C UPTRAVI SELEXIPAG 1 UNK 0
127668962 12766896 4 C CELLCEPT MYCOPHENOLATE MOFETILMYCOPHENOLATE MOFETIL HYDROCHLORIDE 1 UNK 0
127668962 12766896 5 C PREDNISONE. PREDNISONE 1 UNK 0
127668962 12766896 6 C LASIX FUROSEMIDE 1 UNK 0
127668962 12766896 7 C ALDACTONE SPIRONOLACTONE 1 UNK 0
127668962 12766896 8 C PARIET RABEPRAZOLE SODIUM 1 UNK 0
127668962 12766896 9 C KCL POTASSIUM CHLORIDE 1 UNK 0
127668962 12766896 10 C MG MAGNESIUM 1 UNK 0
127668962 12766896 11 C CALCIUM CALCIUM 1 UNK 0
127668962 12766896 12 C VITAMIN D CHOLECALCIFEROL 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127668962 12766896 1 Pulmonary arterial hypertension
127668962 12766896 2 Connective tissue disorder

Outcome of event

Event ID CASEID OUTC COD
127668962 12766896 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127668962 12766896 Pain in jaw
127668962 12766896 Pneumonia

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found