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
119267826 11926782 6 F 20151101 20160824 20160119 20160831 EXP CA-PFIZER INC-2016014677 PFIZER 81.00 YR M Y 66.67000 KG 20160831 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
119267826 11926782 1 PS REVATIO SILDENAFIL CITRATE 1 Oral 20 MG, 3X/DAY 21845 20 MG FILM-COATED TABLET TID
119267826 11926782 2 C METOPROLOL. METOPROLOL 1 UNK 0
119267826 11926782 3 C VITAMIN B12 CYANOCOBALAMIN 1 UNK 0
119267826 11926782 4 C PREDNISONE. PREDNISONE 1 UNK 0
119267826 11926782 5 C TECTA PANTOPRAZOLE MAGNESIUM 1 UNK 0
119267826 11926782 6 C VITAMIN D CHOLECALCIFEROL 1 UNK 0
119267826 11926782 7 C SINGULAIR MONTELUKAST SODIUM 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119267826 11926782 1 Pulmonary arterial hypertension

Outcome of event

Event ID CASEID OUTC COD
119267826 11926782 OT
119267826 11926782 DE
119267826 11926782 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
119267826 11926782 Condition aggravated
119267826 11926782 Death
119267826 11926782 Dyspnoea
119267826 11926782 Haemorrhage
119267826 11926782 Laryngitis
119267826 11926782 Peripheral swelling
119267826 11926782 Thyroid cancer

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
119267826 11926782 1 20150710 0