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
100635507 10063550 7 F 200512 20160812 20140407 20160819 EXP US-009507513-1404USA001685 MERCK 0.00 F Y 40.82000 KG 20160819 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
100635507 10063550 1 PS SINGULAIR MONTELUKAST SODIUM 1 Oral 10 MG, QD 20829 10 MG TABLET QD
100635507 10063550 2 SS SINGULAIR MONTELUKAST SODIUM 1 Oral 10 MG, QD 20829 10 MG TABLET QD
100635507 10063550 3 SS SINGULAIR MONTELUKAST SODIUM 1 Oral UNK UNK, UNKNOWN 20829 TABLET
100635507 10063550 4 SS SINGULAIR MONTELUKAST SODIUM 1 20829 TABLET
100635507 10063550 5 C ADVAIR HFA FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Unknown UNK, UNKNOWN U 0
100635507 10063550 6 C PREDNISONE. PREDNISONE 1 Unknown UNK, UNKNOWN U 0 TABLET
100635507 10063550 7 C EFFEXOR VENLAFAXINE HYDROCHLORIDE 1 Unknown UNK, UNKNOWN U 0
100635507 10063550 8 C XANAX ALPRAZOLAM 1 Unknown UNK, UNKNOWN U 0
100635507 10063550 9 C ZOFRAN ONDANSETRON HYDROCHLORIDE 1 Unknown UNK, UNKNOWN U 0
100635507 10063550 10 C PERCOCET ACETAMINOPHENOXYCODONE HYDROCHLORIDE 1 Unknown UNK, UNKNOWN U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
100635507 10063550 1 Asthma
100635507 10063550 2 Hypersensitivity
100635507 10063550 3 Asthma
100635507 10063550 4 Hypersensitivity
100635507 10063550 5 Product used for unknown indication
100635507 10063550 6 Product used for unknown indication
100635507 10063550 7 Product used for unknown indication
100635507 10063550 8 Product used for unknown indication
100635507 10063550 9 Product used for unknown indication
100635507 10063550 10 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
100635507 10063550 OT
100635507 10063550 HO
100635507 10063550 DS
100635507 10063550 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
100635507 10063550 Abasia
100635507 10063550 Adverse event
100635507 10063550 Amnesia
100635507 10063550 Asthenia
100635507 10063550 Asthma
100635507 10063550 Cardiac disorder
100635507 10063550 Cardiomyopathy
100635507 10063550 Cellulitis
100635507 10063550 Colostomy
100635507 10063550 Colostomy closure
100635507 10063550 Deep vein thrombosis
100635507 10063550 Depression
100635507 10063550 Diverticulitis
100635507 10063550 Eosinophilic granulomatosis with polyangiitis
100635507 10063550 Eye oedema
100635507 10063550 Flatulence
100635507 10063550 Gait deviation
100635507 10063550 Gastric disorder
100635507 10063550 Gastrointestinal surgery
100635507 10063550 Gastrointestinal tube insertion
100635507 10063550 Lip oedema
100635507 10063550 Loss of control of legs
100635507 10063550 Lung infiltration
100635507 10063550 Mass excision
100635507 10063550 Muscular weakness
100635507 10063550 Myocardial infarction
100635507 10063550 Neuralgia
100635507 10063550 Neuropathy peripheral
100635507 10063550 Nightmare
100635507 10063550 Pain
100635507 10063550 Pain in extremity
100635507 10063550 Pancreatitis acute
100635507 10063550 Peroneal nerve palsy
100635507 10063550 Pneumonia
100635507 10063550 Pulmonary mass
100635507 10063550 Quality of life decreased
100635507 10063550 Sleep apnoea syndrome
100635507 10063550 Stress
100635507 10063550 Surgery

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
100635507 10063550 1 20050916 2011 0
100635507 10063550 2 2012 0
100635507 10063550 3 20130320 2013 0