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Index of reports
> Cases resulting in a serious event (40)
> Cases with Blood Creatinine Increased (11)
Below is the selection of adverse event reports related to Esidrix (Hydrochlorothiazide) that includes cases resulting in a serious event where reactions include blood creatinine increased.
Adverse event in 98 year old male receiving Esidrix (Hydrochlorothiazide)
Reported by a individual with unspecified qualification from France on 2007-10-17
Patient: 98 year old male
Adverse reactions / side effects: Bedridden, Blood Creatine Phosphokinase Increased, Blood Urea Increased, Rhabdomyolysis, Cardioactive Drug Level Above Therapeutic, Hypotension, Fall, Malaise, Renal Failure, Fluid Replacement, Dehydration, Myoglobin Blood Increased, Blood Creatinine Increased, Physical Disability
Adverse event resulted in: hospitalization
Suspect drug(s):
Esidrix
Dosage: 25 mg, qd
Administration route: Oral
End date: 2006-03-01
Lasix
Dosage: 60 mg, qd
Administration route: Oral
End date: 2006-03-01
Perindopril Erbumine
Dosage: 4 mg, qd
Administration route: Oral
End date: 2006-03-01
Digoxin
Dosage: 0.125 mg, qw4
Administration route: Oral
End date: 2006-03-01
Other drugs received by patient: Kardegic
Adverse event in 69 year old male receiving Esidrix (Hydrochlorothiazide)
Reported by a individual with unspecified qualification from Norway on 2007-10-17
Patient: 69 year old male
Adverse reactions / side effects: Abdominal Pain, Drug Interaction, Lactic Acidosis, Hyperventilation, Nephrolithiasis, Renal Failure, Catheter Placement, Diarrhoea, Visual Disturbance, Circulatory Collapse, Respiratory Arrest, Blood Creatinine Increased
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Losartan Potassium
Dosage: 50 mg, unk
Indication: Hypertension
Metformin HCL
Indication: Type 2 Diabetes Mellitus
Esidrix
Dosage: 12.5 mg, unk
Indication: Hypertension
Adverse event in 69 year old male receiving Esidrix (Hydrochlorothiazide)
Reported by a individual with unspecified qualification from Norway on 2007-10-16
Patient: 69 year old male
Adverse reactions / side effects: Abdominal Pain, Drug Interaction, Lactic Acidosis, Hyperventilation, Nephrolithiasis, Renal Failure, Catheter Placement, Diarrhoea, Visual Disturbance, Circulatory Collapse, Respiratory Arrest, Blood Creatinine Increased
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Losartan Potassium
Dosage: 50 mg, unk
Indication: Hypertension
Metformin
Indication: Type 2 Diabetes Mellitus
Esidrix
Dosage: 12.5 mg, unk
Indication: Hypertension
Adverse event in 35 year old female receiving Esidrix (Hydrochlorothiazide)
Reported by a individual with unspecified qualification from France on 2007-06-05
Patient: 35 year old female, weighing 78.0 kg (171.6 pounds)
Adverse reactions / side effects: Creatinine Renal Clearance Decreased, Vomiting, Nausea, Condition Aggravated, Hepatitis, Dehydration, Proteinuria, Blood Creatinine Increased, Asthenia, Muscle Spasms, Renal Failure Acute
Adverse event resulted in: hospitalization
Suspect drug(s):
Lasix
Dosage: 250 mg, qd
Administration route: Oral
Start date: 2007-01-23
End date: 2007-02-16
Esidrix
Dosage: 25 mg, qd
Administration route: Oral
Start date: 2007-01-23
End date: 2007-02-16
Odrik
Dosage: 0.5 mg, qd
Administration route: Oral
End date: 2007-02-11
Odrik
Dosage: 2 mg, qd
Administration route: Oral
Start date: 2007-02-12
End date: 2007-02-14
Other drugs received by patient: Levemir; Novorapid; Omeprazole; Calcidia; Rifinah; Laroxyl; Aranesp
Adverse event in 65 year old female receiving Esidrix (Hydrochlorothiazide)
Reported by a individual with unspecified qualification from France on 2007-05-31
Patient: 65 year old female, weighing 51.0 kg (112.2 pounds)
Adverse reactions / side effects: Nausea, Hyponatraemia, Condition Aggravated, Hypokalaemia, Loss of Consciousness, Renal Impairment, Malaise, Anorexia, Bradycardia, Blood Creatinine Increased, Asthenia
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Esidrix (Hydrochlorothiazide)
Other drugs received by patient: Lasix; Cellcept; Cortancyl; Cardensiel; Triatec; Cozaar; Levothyroxine Sodium; Mediator; Omeprazole; Plavix; Fosamax; Prograf; DI-Antalvic; Noroxin; Insulin
Adverse event in 65 year old female receiving Esidrix (Hydrochlorothiazide)
Reported by a individual with unspecified qualification from France on 2007-05-31
Patient: 65 year old female, weighing 51.0 kg (112.2 pounds)
Adverse reactions / side effects: Nausea, Hyponatraemia, Condition Aggravated, Hypokalaemia, Loss of Consciousness, Renal Impairment, Malaise, Anorexia, Bradycardia, Blood Creatinine Increased, Asthenia
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Esidrix (Hydrochlorothiazide)
Other drugs received by patient: Lasix; Cellcept; Cortancyl; Cardensiel; Triatec; Cozaar; Levothyroxine Sodium; Mediator; Omeprazole; Plavix; Fosamax; Prograf; DI-Antalvic; Noroxin; Insulin
Adverse event in 35 year old female receiving Esidrix (Hydrochlorothiazide)
Reported by a individual with unspecified qualification from France on 2007-04-30
Patient: 35 year old female, weighing 78.0 kg (171.6 pounds)
Adverse reactions / side effects: Creatinine Renal Clearance Decreased, Vomiting, Nausea, Condition Aggravated, Hepatitis, Dehydration, Proteinuria, Blood Creatinine Increased, Asthenia, Muscle Spasms, Renal Failure Acute
Adverse event resulted in: hospitalization
Suspect drug(s):
Lasix
Dosage: 250 mg, qd
Administration route: Oral
Start date: 2007-01-23
End date: 2007-02-16
Esidrix
Dosage: 25 mg, qd
Administration route: Oral
Start date: 2007-01-23
End date: 2007-02-16
Odrik
Dosage: 0.5 mg, qd
Administration route: Oral
End date: 2007-02-11
Odrik
Dosage: 2 mg, qd
Administration route: Oral
Start date: 2007-02-12
End date: 2007-02-14
Adverse event in 65 year old female receiving Esidrix (Hydrochlorothiazide)
Reported by a individual with unspecified qualification from France on 2007-04-20
Patient: 65 year old female, weighing 51.0 kg (112.2 pounds)
Adverse reactions / side effects: Nausea, Hyponatraemia, Hypokalaemia, Loss of Consciousness, Renal Impairment, Malaise, Anorexia, Bradycardia, Asthenia, Blood Creatinine Increased
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Esidrix (Hydrochlorothiazide)
Other drugs received by patient: Lasix; Cellcept; Cortancyl; Cardensiel; Triatec; Cozaar; Levothyroxine Sodium; Mediator; Omeprazole; Plavix; Fosamax; Prograf; DI-Antalvic; Noroxin; Insulin
Adverse event in 92 year old male receiving Esidrix (Hydrochlorothiazide)
Reported by a individual with unspecified qualification from France on 2007-04-19
Patient: 92 year old male, weighing 70.0 kg (154.0 pounds)
Adverse reactions / side effects: Weight Decreased, Creatinine Renal Clearance Decreased, LIP DRY, Tongue DRY, General Physical Health Deterioration, Dark Circles Under Eyes, Thirst, Renal Failure, Dehydration, Anorexia, Dizziness, Vision Blurred, Blood Creatinine Increased, Asthenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Esidrix
Dosage: 25 mg, qd
Administration route: Oral
Indication: Oedema Peripheral
Start date: 2007-01-01
Lasix
Administration route: Oral
Indication: Oedema Peripheral
Start date: 2007-01-01
Other drugs received by patient: Digoxin; Didronel; Perindopril Erbumine; Nexium; Cortancyl; Cacit D3; Xanax; Zolpidem; Clamoxyl; Aluminum Hydroxide and Magnesium Trisilicate
Adverse event in 86 year old male receiving Esidrix (Hydrochlorothiazide)
Reported by a individual with unspecified qualification from France on 2007-02-09
Patient: 86 year old male
Adverse reactions / side effects: 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
Adverse event in 43 year old female receiving Esidrix (Hydrochlorothiazide)
Reported by a physician from Germany on 2007-01-19
Patient: 43 year old female, weighing 75.0 kg (165.0 pounds)
Adverse reactions / side effects: 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
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