REPORTS OF SIDE EFFECTS / ADVERSE REACTIONS RELATED TO ESIDRIX
Below is a sample of reports where side effects / adverse reactions may be related to Esidrix. The information is not vetted and should not be cosidered as verified clinical evidence.
Possible Esidrix side effects / adverse reactions in 43 year old female
Reported by a physician from Germany on 2007-01-19
Patient: 43 year old female weighing 75.0 kg (165.0 pounds)
Reactions: Renal Impairment, Fatigue, Renal Failure, Diarrhoea, Nausea, Oedema Peripheral, Drug Interaction, Immunosuppressant Drug Level Increased, Blood Creatinine Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Enalapril Maleate
Esidrix
Certican
Dosage: 0.75 mg, bid
Indication: Lung Transplant
Start date: 2005-04-19
Certican
Dosage: 0.125 mg
Neoral
Dosage: 100 mg, bid
Indication: Lung Transplant
Neoral
Dosage: 30 mg, bid
Neoral
Dosage: 25 mg
Cotrim
Start date: 2005-03-23
Other drugs received by patient possibly interacting with the suspect drug: Sempera
Start date: 2005-03-21
Ciprofloxacin
Other drugs received by patient: Decortin-H
Possible Esidrix side effects / adverse reactions in 86 year old male
Reported by a individual with unspecified qualification from France on 2007-02-09
Patient: 86 year old male
Reactions: Vomiting, Ileus, Blood Creatinine Increased, Constipation, Hypokalaemia, Renal Failure Acute
Adverse event resulted in: hospitalization
Suspect drug(s):
Burinex
Dosage: 10 mg/day
Administration route: Oral
Start date: 2005-01-01
End date: 2006-11-17
Esidrix
Dosage: 25 mg, qd
Administration route: Oral
Indication: Hypertension
Start date: 2006-08-10
End date: 2006-11-17
Other drugs received by patient: Mono-Tildiem; Hyperium
Possible Esidrix side effects / adverse reactions in 82 year old male
Reported by a individual with unspecified qualification from France on 2007-02-09
Patient: 82 year old male
Reactions: White Blood Cell Count Decreased, Gastrointestinal Haemorrhage, Anaemia, Pancytopenia, Purpura, Diverticulum Intestinal, Liver Disorder, Gastritis, Pancreatic Disorder, RED Blood Cell Count Decreased, Platelet Count Decreased
Adverse event resulted in: hospitalization
Suspect drug(s):
Voltaren
Administration route: Oral
Esidrix
Dosage: 25 mg, qd
Administration route: Oral
Fucidine CAP
Dosage: 500 mg, bid
Administration route: Oral
Indication: Varicose Ulceration
Start date: 2006-10-08
End date: 2006-10-25
Flammazine
Administration route: Topical
Triatec
Dosage: 5 mg, qd
Administration route: Oral
Other drugs received by patient: Virlix; Biafine; Doliprane
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