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Hydrodiuril (Hydrochlorothiazide) - Reports of Side Effects & Adverse Reactions

 



This is an index of reports of adverse events (side effects, adverse reactions, etc.) related to Hydrodiuril (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 (35)
     Renal Failure Acute (6)Urinary Tract Infection (5)Renal Failure (5)more >>

Cases resulting in a serious event (35)
     Renal Failure Acute (6)Urinary Tract Infection (5)Renal Failure (5)more >>

Cases resulting in death (4)
     Photosensitivity Reaction (3)Cardiac Failure Chronic (3)Melanodermia (3)more >>

Cases resulting in life threatening events (5)
     Vomiting (3)Blood Potassium Increased (3)Diarrhoea (3)more >>

Cases resulting in hospitalization (22)
     Renal Failure Acute (6)Urinary Tract Infection (5)Renal Failure (5)more >>

Cases resulting in other serious reactions (5)
     Anaemia (2)Swollen Tongue (2)Hyperparathyroidism (2)more >>

Below is a sample of reports where side effects / adverse reactions may be related to Hydrodiuril (Hydrochlorothiazide). For a complete list and/or a specific selection of reports, please use the links in the index above.

Adverse event in 69 year old female receiving Hydrodiuril (Hydrochlorothiazide)

Reported by a pharmacist from Canada on 2007-10-18

Patient: 69 year old female, weighing 68.0 kg (149.6 pounds)

Adverse reactions / side effects: Diarrhoea, Urinary Tract Infection, Hyponatraemia

Adverse event resulted in: hospitalization

Suspect drug(s):
Hydrodiuril
    Administration route: Oral

Enbrel
    Indication: Rheumatoid Arthritis
    Start date: 2006-08-01

Other drugs received by patient: Celecoxib; Xalatan; Actonel; Levothyroxine Sodium; Sulfasalazine; Calcium Carbonate



Adverse event in 66 year old female receiving Hydrodiuril (Hydrochlorothiazide)

Reported by a physician from United States on 2007-07-25

Patient: 66 year old female

Adverse reactions / side effects: Hyperparathyroidism, Anaemia, Colitis, Renal Tubular Necrosis, Hypertension, Renal Failure Chronic, Nephropathy

Suspect drug(s):
Prinivil
    Administration route: Oral
    Indication: Hypertension

Hydrodiuril
    Administration route: Oral
    Indication: Hypertension

Sodium Phosphate, Dibasic
    Administration route: Oral
    Indication: Bowel Preparation

Radiographic Contrast Medium (Unspecified)



Adverse event in 78 year old male receiving Hydrodiuril (Hydrochlorothiazide)

Reported by a physician from Japan on 2007-07-24

Patient: 78 year old male

Adverse reactions / side effects: Hypotension, Drug Interaction, Loss of Consciousness

Adverse event resulted in: hospitalization

Suspect drug(s):
Enalapril Maleate
    Dosage: 5 mg qd oral
    Administration route: Oral
    Indication: Hypertension
    Start date: 2006-02-01
    End date: 2007-05-08

Hydrodiuril
    Dosage: 25 mg qd oral
    Administration route: Oral
    Indication: Hypertension
    Start date: 2006-02-01
    End date: 2007-05-08

Norvasc
    Dosage: 5 mg qd oral
    Administration route: Oral
    Indication: Hypertension
    Start date: 2006-02-01

Other drugs received by patient: Magnesium Oxide; Pletal



Adverse event in 66 year old female receiving Hydrodiuril (Hydrochlorothiazide)

Reported by a physician from United States on 2007-07-17

Patient: 66 year old female

Adverse reactions / side effects: Hyperparathyroidism, Anaemia, Colitis, Renal Tubular Necrosis, Hypertension, Nephropathy

Suspect drug(s):
Prinivil
    Administration route: Oral
    Indication: Hypertension

Hydrodiuril
    Administration route: Oral
    Indication: Hypertension

Sodium Phosphate, Dibasic
    Administration route: Oral
    Indication: Bowel Preparation

Radiographic Contrast Medium (Unspecified)



Adverse event in 84 year old male receiving Hydrodiuril (Hydrochlorothiazide)

Reported by a physician from Japan on 2007-07-17

Patient: 84 year old male, weighing 55.0 kg (121.0 pounds)

Adverse reactions / side effects: Liver Disorder

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Hydrodiuril (Hydrochlorothiazide)

Other drugs received by patient: Blopress



Adverse event in 71 year old male receiving Hydrodiuril (Hydrochlorothiazide)

Reported by a physician from Japan on 2007-07-05

Patient: 71 year old male

Adverse reactions / side effects: Liver Disorder

Adverse event resulted in: hospitalization

Suspect drug(s):
Hydrodiuril (Hydrochlorothiazide)

Other drugs received by patient: Blopress



Adverse event in receiving Hydrodiuril (Hydrochlorothiazide)

Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-06-29

Patient:

Adverse reactions / side effects: Pulmonary Valve Stenosis, Multiple Congenital Abnormalities

Suspect drug(s):
Prinivil
    Indication: Hypertension
    Start date: 1990-07-06
    End date: 1990-09-01

Ascorbic Acid

Ferrous Sulfate

Folic Acid

Hydrodiuril

Niacinamide

Pyridoxine Hydrochloride

Riboflavin

Thiamine Mononitrate



Adverse event in 43 year old male receiving Hydrodiuril (Hydrochlorothiazide)

Reported by a physician from Netherlands on 2007-06-05

Patient: 43 year old male

Adverse reactions / side effects: Drug Ineffective

Adverse event resulted in: hospitalization

Suspect drug(s):
Hydrodiuril
    Administration route: Oral
    Indication: Hypertension

Vasotec
    Administration route: Oral
    Indication: Hypertension

Atenolol
    Administration route: Oral

Nifedipine
    Administration route: Oral



Adverse event in 78 year old male receiving Hydrodiuril (Hydrochlorothiazide)

Reported by a physician from Switzerland on 2007-06-01

Patient: 78 year old male

Adverse reactions / side effects: Blood Potassium Abnormal, Ventricular Tachycardia

Adverse event resulted in: life threatening event

Suspect drug(s):
Hydrodiuril (Hydrochlorothiazide)

Other drugs received by patient: Atenolol; Pantoprazole; Aspirin; Isosorbide Mononitrate; Spironolactone; Amiloride; Furosemide



Adverse event in receiving Hydrodiuril (Hydrochlorothiazide)

Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-05-30

Patient:

Adverse reactions / side effects: Pulmonary Valve Stenosis, Multiple Congenital Abnormalities

Suspect drug(s):
Prinivil
    Indication: Hypertension
    Start date: 1990-07-06
    End date: 1990-09-01

Ascorbic Acid

Ferrous Sulfate

Folic Acid

Hydrodiuril

Niacinamide

Pyridoxine Hydrochloride

Riboflavin

Thiamine Mononitrate



Adverse event in receiving Hydrodiuril (Hydrochlorothiazide)

Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-05-22

Patient:

Adverse reactions / side effects: Pulmonary Valve Stenosis, Multiple Congenital Abnormalities

Suspect drug(s):
Prinivil
    Indication: Hypertension
    Start date: 1990-07-06
    End date: 1990-09-01

Ascorbic Acid

Ferrous Sulfate

Folic Acid

Hydrodiuril

Niacinamide

Pyridoxine Hydrochloride

Riboflavin

Thiamine Mononitrate



Adverse event in 43 year old male receiving Hydrodiuril (Hydrochlorothiazide)

Reported by a physician from Netherlands on 2007-05-16

Patient: 43 year old male

Adverse reactions / side effects: Drug Ineffective, Drug Level Decreased

Adverse event resulted in: hospitalization

Suspect drug(s):
Hydrodiuril
    Administration route: Oral
    Indication: Hypertension

Vasotec
    Administration route: Oral
    Indication: Hypertension

Atenolol
    Administration route: Oral

Nifedipine
    Administration route: Oral



Adverse event in 46 year old male receiving Hydrodiuril (Hydrochlorothiazide)

Reported by a physician from United States on 2007-04-24

Patient: 46 year old male

Adverse reactions / side effects: Copper Deficiency, Anaemia, Poisoning, Febrile Neutropenia, Neutropenia

Adverse event resulted in: hospitalization

Suspect drug(s):
Hydrodiuril
    Administration route: Oral
    End date: 2004-05-01

Acetaminophen
    End date: 2004-05-01

Cephalexin

Aspirin
    End date: 2004-05-01

Zinc (Unspecified)

Metoprolol Tartrate
    End date: 2004-05-01

Other drugs received by patient: Methadone Hydrochloride; Diazepam; Methocarbamol; Hydrocodone Bitartrate; Furosemide; Cyanocobalamin; Vitamins (Unspecified); Vitamin A; Calcium Citrate; Ascorbic Acid



Adverse event in 70 year old female receiving Hydrodiuril (Hydrochlorothiazide)

Reported by a physician from United States on 2007-04-24

Patient: 70 year old female

Adverse reactions / side effects: Intraocular Pressure Increased, Angle Closure Glaucoma

Suspect drug(s):
Hydrodiuril (Hydrochlorothiazide)

Other drugs received by patient: Estrogens (Unspecified); Aspirin



Adverse event in 72 year old female receiving Hydrodiuril (Hydrochlorothiazide)

Reported by a individual with unspecified qualification from United Kingdom on 2007-04-05

Patient: 72 year old female

Adverse reactions / side effects: Vomiting, Diarrhoea, Blood Potassium Increased, Continuous Haemodiafiltration, Blood Creatinine Increased, Lethargy, Renal Failure Acute

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Zestril
    Administration route: Oral
    Indication: Hypertension

Hydrodiuril
    Administration route: Oral
    Indication: Hypertension
    End date: 2007-03-03

Other drugs received by patient: Amlodipine Besylate; Atorvastatin Calcium; Lantus; Metformin



Adverse event in 72 year old receiving Hydrodiuril (Hydrochlorothiazide)

Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-04-04

Patient: 72 year old

Adverse reactions / side effects: Vomiting, Diarrhoea, Blood Potassium Increased, Blood Creatinine Increased, Lethargy, Renal Failure Acute

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Hydrodiuril
    Administration route: Oral
    Indication: Hypertension
    End date: 2007-03-03

Prinivil
    Administration route: Oral
    Indication: Hypertension

Other drugs received by patient: Amlodipine Besylate; Atorvastatin Calcium; Lantus; Metformin



Adverse event in 72 year old female receiving Hydrodiuril (Hydrochlorothiazide)

Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-03-30

Patient: 72 year old female

Adverse reactions / side effects: Vomiting, Diarrhoea, Blood Potassium Increased, Blood Creatinine Increased, Lethargy, Renal Failure Acute

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Hydrodiuril
    Administration route: Oral
    Indication: Hypertension
    End date: 2007-03-03

Prinivil
    Administration route: Oral
    Indication: Hypertension

Other drugs received by patient: Amlodipine Besylate; Atorvastatin Calcium; Insulin Glargine; Metformin



Adverse event in 75 year old male receiving Hydrodiuril (Hydrochlorothiazide)

Reported by a health professional (non-physician/pharmacist) from United States on 2007-03-29

Patient: 75 year old male

Adverse reactions / side effects: Renal Failure, Coagulopathy, Urosepsis

Adverse event resulted in: hospitalization

Suspect drug(s):
Prinivil
    Administration route: Oral
    Indication: Hypertension
    Start date: 1999-01-01

Coumadin
    Administration route: Oral
    Start date: 2007-02-07

Hydrodiuril
    Administration route: Oral
    Indication: Polyuria
    Start date: 1999-01-01
    End date: 2007-02-22

Other drugs received by patient: Aspirin; Sulfamethoxazole + Trimethoprim



Adverse event in 75 year old male receiving Hydrodiuril (Hydrochlorothiazide)

Reported by a individual with unspecified qualification from United States on 2007-03-27

Patient: 75 year old male

Adverse reactions / side effects: Coagulopathy, FAT Embolism, Hypotension, Urinary Tract Infection, Headache, Malaise, Renal Failure, Urosepsis, Acute Prerenal Failure, Hypovolaemia

Adverse event resulted in: hospitalization

Suspect drug(s):
Prinivil
    Dosage: unk/unk/po
    Administration route: Oral
    Indication: Hypertension
    Start date: 1999-01-01
    End date: 2007-02-22

Prinivil
    Dosage: unk/unk/po
    Administration route: Oral
    Indication: Hypertension
    Start date: 2007-02-23

Coumadin
    Dosage: 5 mg/daily/unk
    Start date: 2007-02-07
    End date: 2007-02-22

Coumadin
    Dosage: 5 mg/daily/unk
    Start date: 2007-02-23

Hydrodiuril
    Dosage: unk/unk/po
    Administration route: Oral
    Indication: Polyuria
    Start date: 1999-01-01
    End date: 2007-02-22

Other drugs received by patient: Aspirin; Sulfamethoxazole (+) Trimethopri



Adverse event in 54 year old male receiving Hydrodiuril (Hydrochlorothiazide)

Reported by a physician from Japan on 2007-03-26

Patient: 54 year old male

Adverse reactions / side effects: Photosensitivity Reaction, Blood Urea Increased, Cardiac Failure Chronic, Melanodermia, Skin Hyperpigmentation, Skin Hypopigmentation, Blood Creatine Increased, Platelet Count Decreased, Skin Atrophy

Adverse event resulted in: death

Suspect drug(s):
Hydrodiuril
    Administration route: Oral
    Indication: Cardiac Failure Chronic
    Start date: 2002-10-14
    End date: 2003-09-22

Hydrodiuril
    Administration route: Oral
    Indication: Univentricular Heart
    Start date: 2002-10-14
    End date: 2003-09-22

Other drugs received by patient: Lasix; Lasix; Blopress; Blopress; Amiodarone Hydrochloride; Amiodarone Hydrochloride; Kalimate; Kalimate; Allopurinol; Allopurinol



Adverse event in 75 year old male receiving Hydrodiuril (Hydrochlorothiazide)

Reported by a individual with unspecified qualification from United States on 2007-03-20

Patient: 75 year old male

Adverse reactions / side effects: Hypotension, FAT Embolism, Coagulopathy, Nephropathy Toxic, Urinary Tract Infection, Headache, Renal Failure, Malaise, Urosepsis, Hypovolaemia, Acute Prerenal Failure

Adverse event resulted in: hospitalization

Suspect drug(s):
Prinivil
    Indication: Hypertension
    Start date: 1999-01-01

Hydrodiuril
    Indication: Diuretic Therapy
    Start date: 1999-01-01
    End date: 2007-02-22

Study (Unspecified)
    Start date: 2007-02-07

Other drugs received by patient: Coumadin; Aspirin



Adverse event in 69 year old male receiving Hydrodiuril (Hydrochlorothiazide)

Reported by a physician from Norway on 2007-03-16

Patient: 69 year old male

Adverse reactions / side effects: Abdominal Pain, Nephrolithiasis, Hyperventilation, Diarrhoea, Visual Disturbance, Respiratory Arrest, Circulatory Collapse, Renal Failure Acute

Adverse event resulted in: hospitalization

Suspect drug(s):
Cozaar
    Administration route: Oral
    Indication: Hypertension

Hydrodiuril
    Administration route: Oral
    Indication: Hypertension

Metformin
    Indication: Diabetes Mellitus non-Insulin-Dependent



Adverse event in 49 year old female receiving Hydrodiuril (Hydrochlorothiazide)

Reported by a physician from Norway on 2007-03-16

Patient: 49 year old female

Adverse reactions / side effects: Metabolic Acidosis, Hypothermia, Hypoglycaemia, Circulatory Collapse, Gastroenteritis, Renal Failure Acute

Adverse event resulted in: hospitalization

Suspect drug(s):
Cozaar
    Administration route: Oral
    Indication: Hypertension

Hydrodiuril
    Administration route: Oral
    Indication: Hypertension

Glyburide
    Indication: Diabetes Mellitus non-Insulin-Dependent

Metformin
    Administration route: Oral
    Indication: Diabetes Mellitus non-Insulin-Dependent



Adverse event in 69 year old female receiving Hydrodiuril (Hydrochlorothiazide)

Reported by a physician from Norway on 2007-03-16

Patient: 69 year old female

Adverse reactions / side effects: Disseminated Intravascular Coagulation, Hypotension, Acidosis, Cerebellar Infarction, Multi-Organ Failure, Respiratory Failure, Cerebral Infarction, Gastroenteritis, Circulatory Collapse, Blindness, Renal Failure Acute

Adverse event resulted in: hospitalization

Suspect drug(s):
Cozaar
    Administration route: Oral
    Indication: Hypertension

Hydrodiuril
    Administration route: Oral
    Indication: Hypertension

Metformin
    Administration route: Oral
    Indication: Diabetes Mellitus non-Insulin-Dependent

Glimepiride
    Indication: Diabetes Mellitus non-Insulin-Dependent



Adverse event in 30 year old male receiving Hydrodiuril (Hydrochlorothiazide)

Reported by a health professional (non-physician/pharmacist) from Canada on 2007-03-15

Patient: 30 year old male

Adverse reactions / side effects: Agranulocytosis, Myelodysplastic Syndrome

Adverse event resulted in: death

Suspect drug(s):
Hydrodiuril
    Administration route: Oral
    Indication: Hypertension

Olanzapine
    Indication: Schizophrenia, Paranoid Type

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