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
124926762 12492676 2 F 201512 20160817 20160623 20160822 EXP US-GLAXOSMITHKLINE-US2016GSK062906 GLAXOSMITHKLINE 74.89 YR F Y 61.00000 KG 20160822 MD 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
124926762 12492676 1 SS KEFLEX CEPHALEXIN 1 Y 0
124926762 12492676 2 SS BENADRYL DIPHENHYDRAMINE HYDROCHLORIDE 1 UNK, U U 0
124926762 12492676 3 PS ADVAIR HFA FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 1 PUFF(S), BID U 21077 1 DF INHALATION POWDER BID
124926762 12492676 4 SS VENTOLIN ALBUTEROL SULFATE 1 U 0
124926762 12492676 5 SS ZANTAC RANITIDINE HYDROCHLORIDE 1 Oral 150 MG, BID U 0 150 MG BID
124926762 12492676 6 SS XANAX ALPRAZOLAM 1 U 0
124926762 12492676 7 SS BETAPACE SOTALOL HYDROCHLORIDE 1 U 0
124926762 12492676 8 SS CORTEF HYDROCORTISONE 1 U 0
124926762 12492676 9 SS LASIX FUROSEMIDE 1 U 0
124926762 12492676 10 SS NITROGLYCERIN. NITROGLYCERIN 1 U 0
124926762 12492676 11 SS POTASSIUM CHLORIDE. POTASSIUM CHLORIDE 1 U 0
124926762 12492676 12 SS LEVOTHYROXINE. LEVOTHYROXINE 1 U 0
124926762 12492676 13 SS XARELTO RIVAROXABAN 1 U 0
124926762 12492676 14 SS Triamcinolone TRIAMCINOLONE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124926762 12492676 1 Product used for unknown indication
124926762 12492676 2 Product used for unknown indication
124926762 12492676 3 Product used for unknown indication
124926762 12492676 4 Product used for unknown indication
124926762 12492676 5 Product used for unknown indication
124926762 12492676 11 Product used for unknown indication
124926762 12492676 14 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
124926762 12492676 HO
124926762 12492676 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124926762 12492676 Anxiety
124926762 12492676 Atrial fibrillation
124926762 12492676 Chest pain
124926762 12492676 Diarrhoea
124926762 12492676 Drug hypersensitivity
124926762 12492676 Dysphagia
124926762 12492676 Dyspnoea
124926762 12492676 Face oedema
124926762 12492676 Fluid overload
124926762 12492676 Headache
124926762 12492676 Hepatic enzyme increased
124926762 12492676 Hypertension
124926762 12492676 Laryngeal oedema
124926762 12492676 Nausea
124926762 12492676 Oedema
124926762 12492676 Pain
124926762 12492676 Rash
124926762 12492676 Right ventricular failure
124926762 12492676 Urticaria
124926762 12492676 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
124926762 12492676 5 201512 0