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This is an index of reports of adverse events (side effects, adverse reactions, etc.) related to Esidrix (Hydrochlorothiazide). Click on the relevant link below to view a selection of reports according to the event's seriousness level and/or the nature of the side effect / adverse reaction. Or scroll down to view a sample of recent reports further on this page.
Our database includes reports from Jan 2007 to Dec 2007. The information is not vetted and should not be cosidered as verified clinical evidence.
All cases (40)
Cases resulting in a serious event (40)
Cases resulting in life threatening events (14)
Cases resulting in hospitalization (35)
Cases resulting in disability (1)
Cases resulting in other serious reactions (7)
Below is a sample of reports where side effects / adverse reactions may be related to Esidrix (Hydrochlorothiazide). For a complete list and/or a specific selection of reports, please use the links in the index above.
Adverse event in male receiving Esidrix (Hydrochlorothiazide)
Reported by a health professional (non-physician/pharmacist) from France on 2007-10-23
Patient: male
Adverse reactions / side effects: Confusional State, Constipation, Faecaloma, Hypertonia
Adverse event resulted in: hospitalization
Suspect drug(s):
Perindopril Erbumine
Dosage: daily dose: 2 milligram(s)
Administration route: Oral
Indication: Hypertension
Start date: 2007-05-24
Skenan
Dosage: daily dose: unknown
Administration route: Oral
Indication: Back Pain
Start date: 2007-05-15
End date: 2007-05-30
Actiskenan
Dosage: daily dose: unknown; 5 mg prn
Administration route: Oral
Indication: Back Pain
Start date: 2007-05-16
End date: 2007-05-30
Modopar
Dosage: daily dose: 125 milligram(s)
Administration route: Oral
Indication: Parkinsonism
Start date: 2007-05-24
Imovane
Dosage: daily dose: .5 dosage form
Administration route: Oral
Indication: Insomnia
Start date: 2007-05-03
Esidrix
Dosage: daily dose: 12.5 milligram(s)
Administration route: Oral
Indication: Hypertension
Start date: 2007-05-17
End date: 2007-05-24
Adverse event in male receiving Esidrix (Hydrochlorothiazide)
Reported by a health professional (non-physician/pharmacist) from France on 2007-10-19
Patient: male
Adverse reactions / side effects: Rhabdomyolysis, Malaise, Renal Failure, Hypotension, Cardioactive Drug Level Increased, Fall
Adverse event resulted in: hospitalization
Suspect drug(s):
Perindopril Erbumine
Dosage: daily dose: 4 milligram(s)
Administration route: Oral
Indication: Ill-Defined Disorder
End date: 2006-03-01
Lasix
Dosage: daily dose: unknown
Administration route: Oral
Indication: Ill-Defined Disorder
End date: 2006-02-28
Lasix
Dosage: daily dose: unknown
Administration route: Oral
Start date: 2006-03-01
Esidrix
Dosage: daily dose: 1 dosage form
Administration route: Oral
Indication: Ill-Defined Disorder
End date: 2006-03-01
Digoxin
Dosage: daily dose: unknown; 0.125 mg x 4/week
Administration route: Oral
Indication: Ill-Defined Disorder
End date: 2006-02-28
Other drugs received by patient: Kardegic
Adverse event in 98 year old male receiving Esidrix (Hydrochlorothiazide)
Reported by a individual with unspecified qualification on 2007-10-17
Patient: 98 year old male
Adverse reactions / side effects: Malaise, Renal Failure, Rhabdomyolysis, Hypotension, Cardioactive Drug Level Increased, Fall
Adverse event resulted in: hospitalization
Suspect drug(s):
Lasilix Retard
Administration route: Oral
End date: 2006-03-01
Esidrix
Administration route: Oral
End date: 2006-03-01
Coversyl / 00790701 /
Administration route: Oral
End date: 2006-03-01
Hemigoxine
Administration route: Oral
End date: 2006-03-01
Other drugs received by patient: Kardegic / 00002703 /
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 49 year old female receiving Esidrix (Hydrochlorothiazide)
Reported by a health professional (non-physician/pharmacist) from Norway on 2007-10-15
Patient: 49 year old female
Adverse reactions / side effects: Metabolic Acidosis, Hypothermia, Hypoglycaemia, Drug Interaction, Lactic Acidosis, Accidental Overdose, Haemodialysis, Blood Lactic Acid Increased, Loss of Consciousness, Hyperventilation, Drug Toxicity, Respiratory Failure, Circulatory Collapse, Gastroenteritis, Renal Failure Acute
Adverse event resulted in: life threatening event
Suspect drug(s):
Losartan Potassium
Dosage: 50 mg, unk
Indication: Hypertension
Metformin
Dosage: 6 g/day
Administration route: Oral
Esidrix
Dosage: 12.5 mg, unk
Indication: Hypertension
Other drugs received by patient: Glibenklamid
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 80 year old female receiving Esidrix (Hydrochlorothiazide)
Reported by a health professional (non-physician/pharmacist) from France on 2007-07-05
Patient: 80 year old female
Adverse reactions / side effects: Hyponatraemia
Suspect drug(s):
Citalopram Hydrobromide
Dosage: 10 mg qd po
Administration route: Oral
Esidrix
Indication: Hypertension
Other drugs received by patient: ACE Inhibitors (Nos)
Adverse event in 78 year old male receiving Esidrix (Hydrochlorothiazide)
Reported by a physician from Germany on 2007-06-25
Patient: 78 year old male, weighing 66.0 kg (145.2 pounds)
Adverse reactions / side effects: Hyponatraemia, Convulsion
Adverse event resulted in: hospitalization
Suspect drug(s):
Trileptal
Dosage: 1500 mg/d (300-600-600)
Administration route: Oral
Indication: Epilepsy
Start date: 2001-06-27
Trileptal
Dosage: 600 mg, tid
Administration route: Oral
Start date: 2002-03-01
Esidrix
End date: 2006-01-01
Other drugs received by patient: Keppra
Adverse event in 64 year old male receiving Esidrix (Hydrochlorothiazide)
Reported by a physician from Germany on 2007-06-18
Patient: 64 year old male
Adverse reactions / side effects: Syncope, Cardiovascular Insufficiency, Dizziness, Blood Pressure Decreased
Adverse event resulted in: hospitalization
Suspect drug(s):
Bisohexal (Ngx)(bisoprolol) Film-Coated Tablet
Dosage: 10 mg daily, oral
Administration route: Oral
Esidrix
Dosage: 12.5 mg daily, oral
Administration route: Oral
Mirtazapine
Dosage: 15 mg daily, oral
Administration route: Oral
Atacand
Dosage: 16 mg daily, oral
Administration route: Oral
Norvasc
Dosage: 5 mg daily, oral
Administration route: Oral
Lyrica
Dosage: see image
Administration route: Oral
Start date: 2006-12-29
End date: 2006-12-30
Lyrica
Dosage: see image
Administration route: Oral
Start date: 2006-12-31
Cymbalta
Dosage: see image
Administration route: Oral
Start date: 2007-01-05
End date: 2007-01-07
Cymbalta
Dosage: see image
Administration route: Oral
Start date: 2007-01-08
End date: 2007-01-10
Other drugs received by patient: Aspirin; Plavix; Simvahexal (Simvastatin); Molsidomine (Molsidomine); Pantozol (Pantoprazole Sodium); Pentaerythiritol Tetranitrate TAB; Decortin (Prednisone); Vigantoletten (Colecalciferol)
Adverse event in 48 year old male receiving Esidrix (Hydrochlorothiazide)
Reported by a physician from Spain on 2007-06-05
Patient: 48 year old male, weighing 98.0 kg (215.6 pounds)
Adverse reactions / side effects: Dysuria, Urinary Tract Infection, Leukocyturia, Pyrexia
Adverse event resulted in: disablity
Suspect drug(s):
Aliskiren / Hctz VS Hctz
Dosage: code not broken
Administration route: Oral
Indication: Essential Hypertension
Start date: 2007-03-19
Esidrix
Dosage: code not broken
Administration route: Oral
Indication: Essential Hypertension
Start date: 2007-02-15
End date: 2007-03-18
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 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 79 year old female receiving Esidrix (Hydrochlorothiazide)
Reported by a health professional (non-physician/pharmacist) from France on 2007-05-04
Patient: 79 year old female
Adverse reactions / side effects: Sepsis, Stevens-Johnson Syndrome
Adverse event resulted in: life threatening event
Suspect drug(s):
Triflucan
Start date: 2006-06-16
End date: 2006-06-19
Arcalion
Administration route: Oral
Start date: 2006-06-01
End date: 2006-06-19
Primperan INJ
Start date: 2006-06-19
End date: 2006-06-19
Desloratadine
Administration route: Oral
Start date: 2006-06-15
End date: 2006-06-19
Esidrix
Adverse event in 41 year old male receiving Esidrix (Hydrochlorothiazide)
Reported by a physician from Germany on 2007-04-30
Patient: 41 year old male, weighing 110.0 kg (242.0 pounds)
Adverse reactions / side effects: Road Traffic Accident, Clavicle Fracture
Adverse event resulted in: hospitalization
Suspect drug(s):
Aliskiren / Hctz VS Hctz
Dosage: code not broken
Administration route: Oral
Indication: Essential Hypertension
Esidrix
Dosage: code not broken
Administration route: Oral
Indication: Essential Hypertension
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 41 year old female receiving Esidrix (Hydrochlorothiazide)
Reported by a physician from India on 2007-04-26
Patient: 41 year old female, weighing 56.0 kg (123.2 pounds)
Adverse reactions / side effects: Gastroenteritis, Electrolyte Imbalance, Alkalosis Hypochloraemic, Asthenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Aliskiren / Hctz
Dosage: code not broken
Administration route: Oral
Indication: Essential Hypertension
Start date: 2007-03-12
Esidrix
Dosage: code not broken
Administration route: Oral
Indication: Essential Hypertension
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 60 year old male receiving Esidrix (Hydrochlorothiazide)
Reported by a health professional (non-physician/pharmacist) from Germany on 2007-04-20
Patient: 60 year old male
Adverse reactions / side effects: Thrombocytopenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Erbitux
Indication: Oropharyngeal Cancer Stage Unspecified
Start date: 2007-03-02
End date: 2007-03-02
Augmentin '125'
Start date: 2007-03-06
End date: 2007-03-12
Actrapid HM
Indication: Diabetes Mellitus
Start date: 2006-09-15
Esidrix
Administration route: Oral
Cordarone
Administration route: Oral
Ogast
Administration route: Oral
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 44 year old male receiving Esidrix (Hydrochlorothiazide)
Reported by a health professional (non-physician/pharmacist) from France on 2007-04-16
Patient: 44 year old male, weighing 100.0 kg (220.0 pounds)
Adverse reactions / side effects: Pancreatitis Acute
Adverse event resulted in: hospitalization
Suspect drug(s):
Atacand
Administration route: Oral
Indication: Essential Hypertension
Start date: 2006-07-19
Esidrix
Administration route: Oral
Indication: Essential Hypertension
Start date: 2006-07-19
End date: 2007-03-05
Allopurinol
Administration route: Oral
Pravastatin Sodium
Administration route: Oral
Indication: Hyperlipidaemia
Start date: 2006-07-19
End date: 2007-03-05
Inipomp
Administration route: Oral
Start date: 2006-07-19
End date: 2007-02-23
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