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
126688521 12668852 1 I 20160812 20160819 20160819 EXP GB-MHRA-EYC 00143576 GB-PFIZER INC-2016388028 PFIZER 74.00 YR M Y 0.00000 20160819 PH GB GB

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
126688521 12668852 1 PS CELECOXIB. CELECOXIB 1 Oral N 20998
126688521 12668852 2 C BEZAFIBRATE BEZAFIBRATE 1 UNK 0
126688521 12668852 3 C GLIPIZIDE. GLIPIZIDE 1 UNK 0
126688521 12668852 4 C LANTUS INSULIN GLARGINE 1 UNK 0
126688521 12668852 5 C NOVORAPID INSULIN ASPART 1 UNK 0
126688521 12668852 6 C OMEPRAZOLE. OMEPRAZOLE 1 UNK 0
126688521 12668852 7 C QUININE QUININE 1 0
126688521 12668852 8 C RAMIPRIL. RAMIPRIL 1 0
126688521 12668852 9 C SOLIFENACIN SOLIFENACIN 1 0
126688521 12668852 10 C TAMSULOSIN TAMSULOSIN 1 0
126688521 12668852 11 C TRAMADOL. TRAMADOL 1 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126688521 12668852 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126688521 12668852 Cardiac failure acute
126688521 12668852 Dyspnoea
126688521 12668852 Oedema peripheral
126688521 12668852 Pleural effusion

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

no results found

Therapies reported

no results found