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
127256171 12725617 1 I 20040105 20160830 20160908 20160908 EXP US-AMGEN-USASL2016116236 AMGEN 0.00 Y 0.00000 20160908 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
127256171 12725617 1 PS PROCRIT ERYTHROPOIETIN 1 Unknown UNK U 103234 UNKNOWN FORMULATION
127256171 12725617 2 C SODIUM CHLORIDE. SODIUM CHLORIDE 1 Intravenous (not otherwise specified) 10 ML, AS NECESSARY (PRN) 0 10 ML
127256171 12725617 3 C SODIUM CHLORIDE. SODIUM CHLORIDE 1 Intravenous (not otherwise specified) 20 ML, AS NECESSARY (PRN) 0 20 ML
127256171 12725617 4 C HEPARIN HEPARIN SODIUM 1 Intravenous (not otherwise specified) UNK UNK, ONE TIME DOSE (100 UNIT/ML) 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127256171 12725617 1 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127256171 12725617 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127256171 12725617 Abdominal pain
127256171 12725617 Abdominal pain upper
127256171 12725617 Anxiety
127256171 12725617 Arthralgia
127256171 12725617 Arthritis
127256171 12725617 Asthma
127256171 12725617 Atrial fibrillation
127256171 12725617 Back pain
127256171 12725617 Bezoar
127256171 12725617 Cardiac pacemaker insertion
127256171 12725617 Central venous catheterisation
127256171 12725617 Chest pain
127256171 12725617 Chronic obstructive pulmonary disease
127256171 12725617 Constipation
127256171 12725617 Device related thrombosis
127256171 12725617 Diaphragmatic hernia, obstructive
127256171 12725617 Diarrhoea
127256171 12725617 Duodenal ulcer
127256171 12725617 Dyspepsia
127256171 12725617 Gastrooesophageal reflux disease
127256171 12725617 Hypertension
127256171 12725617 Hypocalcaemia
127256171 12725617 Hypokalaemia
127256171 12725617 Hypothyroidism
127256171 12725617 Impaired gastric emptying
127256171 12725617 Infrequent bowel movements
127256171 12725617 Iron deficiency anaemia
127256171 12725617 Oesophageal achalasia
127256171 12725617 Oesophageal stenosis
127256171 12725617 Osteoporosis
127256171 12725617 Palpitations
127256171 12725617 Presyncope
127256171 12725617 Sinus tachycardia
127256171 12725617 Thalassaemia beta
127256171 12725617 Tricuspid valve incompetence
127256171 12725617 Ventricular extrasystoles
127256171 12725617 Vitamin D deficiency
127256171 12725617 Vomiting
127256171 12725617 Weight decreased

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
127256171 12725617 2 20160830 0
127256171 12725617 3 20160830 0
127256171 12725617 4 20160830 0