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
123934629 12393462 9 F 2003 20160920 20160523 20160923 EXP US-GLAXOSMITHKLINE-US2016070960 GLAXOSMITHKLINE 52.25 YR F Y 0.00000 20160923 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
123934629 12393462 1 PS CEFTIN CEFUROXIME AXETIL 1 Oral 10 ML, BID Y C760366 50672 10 ML ORAL SUSPENSION BID
123934629 12393462 2 SS CEFTIN CEFUROXIME AXETIL 1 Oral 500 MG, BID Y 0 500 MG TABLET BID
123934629 12393462 3 SS SEREVENT DISKUS SALMETEROL XINAFOATE 1 Respiratory (inhalation) 1 PUFF(S), BID 0 1 DF INHALATION POWDER BID
123934629 12393462 4 SS VENTOLIN HFA ALBUTEROL SULFATE 1 Respiratory (inhalation) 2 PUFF(S), PRN 0 2 DF
123934629 12393462 5 SS PULMICORT TURBUHALER BUDESONIDE 1 UNK U 0
123934629 12393462 6 C PROTONIX PANTOPRAZOLE SODIUM 1 0
123934629 12393462 7 C MAGNESIUM MAGNESIUM 1 0
123934629 12393462 8 C MYSOLINE PRIMIDONE 1 0
123934629 12393462 9 C PEPCID AC FAMOTIDINE 1 0
123934629 12393462 10 C ASPIRIN (BABY) ASPIRIN 1 0
123934629 12393462 11 C DUONEB ALBUTEROL SULFATEIPRATROPIUM BROMIDE 1 0
123934629 12393462 12 C LEVOXYL LEVOTHYROXINE SODIUM 1 0
123934629 12393462 13 C KLONOPIN CLONAZEPAM 1 0
123934629 12393462 14 C ZETIA EZETIMIBE 1 0
123934629 12393462 15 C VICODIN ACETAMINOPHENHYDROCODONE BITARTRATE 1 0
123934629 12393462 16 C ATIVAN LORAZEPAM 1 0
123934629 12393462 17 C LIPITOR ATORVASTATIN CALCIUM 1 0
123934629 12393462 18 C VITAMIN B12 CYANOCOBALAMIN 1 0
123934629 12393462 19 C VITAMIN D3 CHOLECALCIFEROL 1 0
123934629 12393462 20 C TYLENOL PM ACETAMINOPHENDIPHENHYDRAMINE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123934629 12393462 1 Product used for unknown indication
123934629 12393462 2 Product used for unknown indication
123934629 12393462 3 Asthma
123934629 12393462 4 Dyspnoea
123934629 12393462 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
123934629 12393462 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123934629 12393462 Abdominal distension
123934629 12393462 Abdominal pain
123934629 12393462 Abdominal pain upper
123934629 12393462 Adverse event
123934629 12393462 Colonoscopy
123934629 12393462 Coma
123934629 12393462 Condition aggravated
123934629 12393462 Diarrhoea
123934629 12393462 Diverticulitis
123934629 12393462 Drug dose omission
123934629 12393462 Fatigue
123934629 12393462 Gastric disorder
123934629 12393462 Gastrointestinal disorder
123934629 12393462 Haematochezia
123934629 12393462 Impaired gastric emptying
123934629 12393462 Lung disorder
123934629 12393462 Malaise
123934629 12393462 Medication error
123934629 12393462 Melaena
123934629 12393462 Mucous stools
123934629 12393462 Multiple allergies
123934629 12393462 Muscle spasms
123934629 12393462 Nausea
123934629 12393462 Pneumonia
123934629 12393462 Product preparation error
123934629 12393462 Product quality issue
123934629 12393462 Reactive gastropathy
123934629 12393462 Respiratory failure
123934629 12393462 Systemic lupus erythematosus

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
123934629 12393462 1 20160517 20160518 0
123934629 12393462 2 20160519 201605 0