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
122765192 12276519 2 F 20160718 20160418 20160728 EXP US-GLAXOSMITHKLINE-A1088526A GLAXOSMITHKLINE 0.00 F Y 0.00000 20160728 CN US US

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
122765192 12276519 1 SS LEVAQUIN LEVOFLOXACIN 1 Unknown U UNKNOWN 0
122765192 12276519 2 SS CLINDAMYCIN CLINDAMYCINCLINDAMYCIN PHOSPHATE 1 Unknown U UNKNOWN 0
122765192 12276519 3 SS SEPTRA SULFAMETHOXAZOLETRIMETHOPRIM 1 Unknown U 0
122765192 12276519 4 SS SYNVISC HYALURONATE SODIUM 1 Unknown U UNKNOWN 0
122765192 12276519 5 PS ADVAIR DISKUS FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 U 5ZP0393 21077 INHALATION POWDER
122765192 12276519 6 SS ADVAIR DISKUS FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 U 21077 INHALATION POWDER

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122765192 12276519 1 Product used for unknown indication
122765192 12276519 2 Product used for unknown indication
122765192 12276519 3 Product used for unknown indication
122765192 12276519 4 Product used for unknown indication
122765192 12276519 5 Asthma
122765192 12276519 6 Chronic obstructive pulmonary disease

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
122765192 12276519 Drug hypersensitivity
122765192 12276519 Incorrect dose administered

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

no results found

Therapies reported

no results found