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
125363072 12536307 2 F 20160602 20160629 20160707 20160712 EXP FR-PFIZER INC-2016323844 PFIZER 64.00 YR M Y 0.00000 20160712 OT FR FR

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
125363072 12536307 1 SS Sevikar AMLODIPINE BESYLATEOLMESARTAN MEDOXOMIL 1 Oral UNK UNK, DAILY (5/40 MG) Y 0 FILM-COATED TABLET
125363072 12536307 2 PS TAHOR ATORVASTATIN CALCIUM 1 Oral 20 MG, DAILY Y 20702 20 MG FILM-COATED TABLET
125363072 12536307 3 SS ALLOPURINOL. ALLOPURINOL 1 Oral 1 DF, DAILY Y 0 1 DF
125363072 12536307 4 SS DIFFU K POTASSIUM CHLORIDE 1 Oral 2 DF, DAILY 0 2 DF CAPSULE

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125363072 12536307 1 Hypertension

Outcome of event

Event ID CASEID OUTC COD
125363072 12536307 OT
125363072 12536307 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125363072 12536307 Acute kidney injury
125363072 12536307 Diarrhoea
125363072 12536307 Dyspnoea
125363072 12536307 Metabolic acidosis

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
125363072 12536307 1 20160614 0
125363072 12536307 2 201606 0
125363072 12536307 3 201606 0