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
125622101 12562210 1 I 20160623 20160704 20160715 20160715 EXP GB-MHRA-EYC 00141755 GB-WATSON-2016-15361 WATSON 70.00 YR M Y 82.55000 KG 20160715 CN 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
125622101 12562210 1 PS TRIMETHOPRIM. TRIMETHOPRIM 1 Oral 200 MG, BID 2800 MG UNCONFIRMED 70049 200 MG TABLET BID
125622101 12562210 2 C SIMVASTATIN. SIMVASTATIN 1 Unknown UNK U 0
125622101 12562210 3 C KETOCONAZOLE. KETOCONAZOLE 1 Unknown UNK U 0
125622101 12562210 4 C SILDENAFIL. SILDENAFIL 1 Unknown UNK U 0
125622101 12562210 5 C LANSOPRAZOLE TEVA LANSOPRAZOLE 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125622101 12562210 1 Urinary tract infection
125622101 12562210 2 Product used for unknown indication
125622101 12562210 3 Product used for unknown indication
125622101 12562210 4 Product used for unknown indication
125622101 12562210 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125622101 12562210 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125622101 12562210 Erythema
125622101 12562210 Malaise
125622101 12562210 Rash maculo-papular

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
125622101 12562210 1 20160620 0