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
127723491 12772349 1 I 20151115 20160831 20160922 20160922 EXP IT-MINISAL02-372768 IT-MYLANLABS-2016M1037645 MYLAN 0.00 Y 0.00000 20160922 MD IT IT

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
127723491 12772349 1 PS CLARITHROMYCIN. CLARITHROMYCIN 1 UNK U U 65195
127723491 12772349 2 SS PANTOPRAZOLE PANTOPRAZOLE SODIUM 1 UNK U U 0
127723491 12772349 3 SS LEVOXACIN LEVOFLOXACIN 1 UNK U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127723491 12772349 1 Helicobacter infection
127723491 12772349 2 Helicobacter infection
127723491 12772349 3 Helicobacter infection

Outcome of event

Event ID CASEID OUTC COD
127723491 12772349 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127723491 12772349 Dyspnoea
127723491 12772349 Erythema
127723491 12772349 Hypersensitivity
127723491 12772349 Palpitations

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
127723491 12772349 1 20151114 0
127723491 12772349 2 20151114 0
127723491 12772349 3 20151114 0