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Index of reports
> All cases (40)
> Cases with Dehydration (8)
Below is the selection of adverse event reports related to Esidrix (Hydrochlorothiazide) that includes all cases where reactions include dehydration.
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 79 year old female receiving Esidrix (Hydrochlorothiazide)
Reported by a physician from France on 2007-07-09
Patient: 79 year old female
Adverse reactions / side effects: General Physical Condition Abnormal, Lupus-Like Syndrome, Fall, Periorbital Haematoma, Loss of Consciousness, Proteinuria, Depression, Sjogren's Syndrome, Renal Failure Acute, Prurigo, Stevens-Johnson Syndrome, White Blood Cell Count Decreased, Biopsy Salivary Gland Abnormal, Hyponatraemia, Staphylococcal Sepsis, Antinuclear Antibody Positive, Conjunctivitis Infective, Rash Erythematous, Dehydration, Asthenia, Anti-SS-A Antibody Positive, Face Injury
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Desloratadine
Dosage: 5 mg; qd; po
Administration route: Oral
Start date: 2006-06-15
End date: 2006-06-19
Arcalion (NO Pref. Name)
Dosage: po
Administration route: Oral
Start date: 2006-06-01
End date: 2006-06-19
Esidrix
End date: 2006-06-19
Primperan TAB
End date: 2006-06-19
Fluconazole
End date: 2006-06-19
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 79 year old female receiving Esidrix (Hydrochlorothiazide)
Reported by a individual with unspecified qualification from France on 2007-05-29
Patient: 79 year old female
Adverse reactions / side effects: Pruritus, Lupus-Like Syndrome, Conjunctivitis, Pyrexia, Hypernatraemia, Fall, Loss of Consciousness, Periorbital Haematoma, C-Reactive Protein Increased, Proteinuria, Blood Uric Acid Increased, Dermatitis Bullous, Injury, Erythema Multiforme, Sjogren's Syndrome, Renal Failure Acute, Stevens-Johnson Syndrome, General Physical Health Deterioration, Staphylococcal Sepsis, Epidermolysis, Antinuclear Antibody Positive, Fluid Replacement, Dehydration, Rash Erythematous, Toxic Skin Eruption, Anti-SS-A Antibody Positive, Inflammation
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Arcalion
Dosage: unk, unk
Administration route: Oral
Indication: Depressive Symptom
Start date: 2006-06-01
End date: 2006-06-19
Primperan INJ
End date: 2006-06-19
Triflucan
End date: 2006-06-19
Desloratadine
Dosage: 1 df, qd
Administration route: Oral
Start date: 2006-06-15
End date: 2006-06-19
Esidrix
Dosage: unk, unk
Administration route: Oral
End date: 2006-06-19
Adverse event in 79 year old female receiving Esidrix (Hydrochlorothiazide)
Reported by a physician from France on 2007-05-04
Patient: 79 year old female
Adverse reactions / side effects: Fall, Loss of Consciousness, Proteinuria, Blood Uric Acid Increased, Eyelid Disorder, Depression, Sjogren's Syndrome, Erythema Multiforme, Haematoma, Renal Failure Acute, Stevens-Johnson Syndrome, White Blood Cell Count Decreased, Toxic Epidermal Necrolysis, Hyponatraemia, Staphylococcal Sepsis, Epidermolysis, Antinuclear Antibody Positive, Conjunctivitis Infective, Sialoadenitis, Dehydration, Asthenia, Anti-SS-A Antibody Positive, Face Injury, Toxic Skin Eruption
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Desloratadine
Dosage: 5 mg; qd; po
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2006-06-15
End date: 2006-06-19
Arcalion (NO Pref. Name)
Dosage: po
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2006-06-01
End date: 2006-06-19
Esidrix
Indication: Drug USE FOR Unknown Indication
End date: 2006-06-19
Primperan TAB
Indication: Drug USE FOR Unknown Indication
End date: 2006-06-19
Fluconazole
Indication: Drug USE FOR Unknown Indication
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 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 92 year old male receiving Esidrix (Hydrochlorothiazide)
Reported by a individual with unspecified qualification on 2007-04-09
Patient: 92 year old male, weighing 70.0 kg (154.0 pounds)
Adverse reactions / side effects: Anorexia, Dehydration, Condition Aggravated, Vision Blurred, Renal Failure Acute
Adverse event resulted in: hospitalization
Suspect drug(s):
Lasilix / 00032601 /
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2007-01-01
Esidrix
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2007-01-01
Other drugs received by patient: Digoxin; Didronel / 00553202 /; Coversyl / 00790701 /; Nexium; Cortancyl; Cacit D3; Xanax; Zolpidem; Clamoxyl / 00249601 /; Smecta / 01255901 /; Diuretics
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