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
125757831 12575783 1 I 201408 20160711 20160720 20160720 EXP DK-DKMA-ADR 23528868 PHHY2016DK095441 SANDOZ 70.00 YR F Y 0.00000 20160720 OT DK DK

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
125757831 12575783 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Oral U 76593
125757831 12575783 2 SS METEX METFORMIN HYDROCHLORIDE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125757831 12575783 1 Respiratory tract infection
125757831 12575783 2 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
125757831 12575783 HO
125757831 12575783 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
125757831 12575783 Activities of daily living impaired
125757831 12575783 Bone marrow failure
125757831 12575783 Candida infection
125757831 12575783 Gastrointestinal tube insertion
125757831 12575783 Hypogeusia
125757831 12575783 Mouth ulceration
125757831 12575783 Oropharyngeal pain
125757831 12575783 Pancytopenia
125757831 12575783 Pyrexia
125757831 12575783 Rash erythematous
125757831 12575783 Renal impairment
125757831 12575783 Scar
125757831 12575783 Swelling
125757831 12575783 Tendon pain
125757831 12575783 Toxic epidermal necrolysis
125757831 12575783 Vomiting

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
125757831 12575783 1 20140806 0
125757831 12575783 2 200710 0