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This is an index of reports of adverse events (side effects, adverse reactions, etc.) related to 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 (242)
Cases resulting in a serious event (229)
Cases resulting in death (22)
Cases resulting in life threatening events (21)
Cases resulting in hospitalization (128)
Cases resulting in disability (2)
Cases resulting in other serious reactions (95)
Below is a sample of reports where side effects / adverse reactions may be related to Hydrochlorothiazide. For a complete list and/or a specific selection of reports, please use the links in the index above.
Adverse event in female receiving Hydrochlorothiazide
Reported by a consumer/non-health professional from United States on 2007-10-30
Patient: female
Adverse reactions / side effects: Osteoarthritis, Overweight
Suspect drug(s):
Hydrochlorothiazide
Dosage: 25 mg, qd
Indication: Hypertension
Benazepril Hydrochloride
Dosage: 1 to 1 1/2 tablet, daily
Indication: Hypertension
Adverse event in male receiving Hydrochlorothiazide
Reported by a individual with unspecified qualification from United States on 2007-10-29
Patient: male
Adverse reactions / side effects: Dysarthria, Facial Paresis, Muscular Weakness
Adverse event resulted in: hospitalization
Suspect drug(s):
Aggrenox
Dosage: blinded study drug
Administration route: Oral
Indication: Cerebrovascular Accident Prophylaxis
Micardis
Dosage: blinded study drug
Administration route: Oral
Indication: Cerebrovascular Accident Prophylaxis
Clopidogrel
Dosage: blinded study drug
Administration route: Oral
Indication: Cerebrovascular Accident Prophylaxis
Placebo (Blind)
Dosage: blinded study drug
Administration route: Oral
Indication: Cerebrovascular Accident Prophylaxis
Hydrochlorothiazide
Indication: Hypertension
Norvasc
Indication: Hypertension
Adverse event in male receiving Hydrochlorothiazide
Reported by a consumer/non-health professional from United States on 2007-10-26
Patient: male
Adverse reactions / side effects: Neuritis
Suspect drug(s):
Lotrel
Indication: Hypertension
Hydrochlorothiazide
Dosage: 25 mg, unk
Indication: Hypertension
Adverse event in 70 year old female receiving Hydrochlorothiazide
Reported by a physician from United States on 2007-10-26
Patient: 70 year old female, weighing 72.9 kg (160.4 pounds)
Adverse reactions / side effects: Facial Palsy, Hyperkalaemia, Headache, Hemiparesis, Fall, Dizziness, Blood Creatinine Increased, Blood Urea Increased, Anaemia, Muscular Weakness, Cerebrovascular Accident, Concomitant Disease Progression, Carotid Artery Stenosis, Renal Failure, Vertigo, Hypertension
Adverse event resulted in: hospitalization
Suspect drug(s):
Lotrel
Dosage: level 1
Administration route: Oral
Indication: Hypertension
Start date: 2004-08-02
Lotrel
Dosage: level 3
Administration route: Oral
Lotrel
Dosage: no treatment
Lotrel
Dosage: level 3
Administration route: Oral
Hydrochlorothiazide
Administration route: Oral
End date: 2007-04-11
Other drugs received by patient: Lipitor; Atenolol; Aspirin; Glipizide; Trazodone HCL; Zoloft; Lantus
Adverse event in female receiving Hydrochlorothiazide
Reported by a individual with unspecified qualification from United States on 2007-10-26
Patient: female
Adverse reactions / side effects: Malaise, Sepsis
Suspect drug(s):
Hydrochlorothiazide
Indication: Hypertension
Amlodipine Besylate
Indication: Hypertension
Atenolol
Indication: Hypertension
Adverse event in 70 year old female receiving Hydrochlorothiazide
Reported by a physician from United States on 2007-10-25
Patient: 70 year old female, weighing 72.9 kg (160.4 pounds)
Adverse reactions / side effects: Facial Palsy, Hyperkalaemia, Headache, Hemiparesis, Fall, Dizziness, Blood Creatinine Increased, Blood Urea Increased, Anaemia, Muscular Weakness, Cerebrovascular Accident, Concomitant Disease Progression, Carotid Artery Stenosis, Renal Failure, Vertigo, Hypertension
Adverse event resulted in: hospitalization
Suspect drug(s):
Lotrel
Dosage: level 1
Administration route: Oral
Indication: Hypertension
Start date: 2004-08-02
Lotrel
Dosage: level 3
Administration route: Oral
Lotrel
Dosage: no treatment
Lotrel
Dosage: level 3
Administration route: Oral
Hydrochlorothiazide
Administration route: Oral
End date: 2007-04-11
Other drugs received by patient: Lipitor; Atenolol; Aspirin; Glipizide; Trazodone HCL; Zoloft; Lantus
Adverse event in receiving Hydrochlorothiazide
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-25
Patient:
Adverse reactions / side effects: Polyp
Suspect drug(s):
Spironolactone RPG 50 MG Comprime Pellicule
Phenytoin
Hydrochlorothiazide
Adverse event in receiving Hydrochlorothiazide
Reported by a pharmacist from United States on 2007-10-24
Patient:
Adverse reactions / side effects: Medication Error, Pharmaceutical Product Complaint
Suspect drug(s):
Hydrochlorothiazide
Allopurinol
Adverse event in 75 year old male receiving Hydrochlorothiazide
Reported by a pharmacist from United States on 2007-10-24
Patient: 75 year old male
Adverse reactions / side effects: Hyponatraemia
Adverse event resulted in: hospitalization
Suspect drug(s):
Hydrochlorothiazide
Adverse event in female receiving Hydrochlorothiazide
Reported by a physician from United States on 2007-10-24
Patient: female, weighing 66.2 kg (145.7 pounds)
Adverse reactions / side effects: Disturbance in Attention, Musculoskeletal Discomfort, Heart Rate Irregular, Blood Sodium Decreased
Suspect drug(s):
Topamax
Administration route: Oral
Topamax
Administration route: Oral
Indication: Drug Therapy
Topamax
Administration route: Oral
Indication: Migraine Prophylaxis
Hydrochlorothiazide
Indication: Drug USE FOR Unknown Indication
Other drugs received by patient: Zoloft; Concerta; Provigil; Lisinopril
Adverse event in 69 year old female receiving Hydrochlorothiazide
Reported by a individual with unspecified qualification from United States on 2007-10-22
Patient: 69 year old female
Adverse reactions / side effects: Electrocardiogram QT Prolonged, Ventricular Extrasystoles, Syncope, Supraventricular Extrasystoles, Hypokalaemia
Adverse event resulted in: hospitalization
Suspect drug(s):
Sotalol Hydrochloride
Administration route: Oral
End date: 2007-09-09
Torem / GFR /
Administration route: Oral
Indication: Diuretic Therapy
End date: 2007-09-09
Metolazone
Administration route: Oral
Indication: Diuretic Therapy
End date: 2007-09-09
Hydrochlorothiazide
Administration route: Oral
Indication: Diuretic Therapy
End date: 2007-09-09
Other drugs received by patient: Marcumar
Adverse event in female receiving Hydrochlorothiazide
Reported by a consumer/non-health professional from United States on 2007-10-19
Patient: female
Adverse reactions / side effects: Drug Exposure During Pregnancy, Blood Pressure Abnormal, PRE-Eclampsia
Adverse event resulted in: life threatening event
Suspect drug(s):
Hydrochlorothiazide
Adverse event in 73 year old female receiving Hydrochlorothiazide
Reported by a physician from United States on 2007-10-19
Patient: 73 year old female
Adverse reactions / side effects: Dyspnoea Exertional, Extrasystoles, Presyncope, Dizziness, Nodal Rhythm, Asthenia, Sinus Bradycardia
Adverse event resulted in: hospitalization
Suspect drug(s):
Metoprolol Tartrate
Dosage: 50 mg; daily;
Indication: Hypertension
Lisinopril
Dosage: 20 mg, daily;
Indication: Hypertension
Hydrochlorothiazide
Dosage: 12.5 mg; twice a day;
Indication: Hypertension
Felodipine
Dosage: 5 mg, daily;
Indication: Hypertension
Clonidine Hydrochloride
Dosage: 0.2 mg; twice a day;
Indication: Hypertension
Diltiazem Hydrochloride
Dosage: 180 mg; daily;
Indication: Hypertension
Adverse event in female receiving Hydrochlorothiazide
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-19
Patient: female, weighing 94.6 kg (208.1 pounds)
Adverse reactions / side effects: Feeling Cold, Renal Failure Acute, Tremor
Adverse event resulted in: hospitalization
Suspect drug(s):
Lyrica
Administration route: Oral
Indication: Neck Pain
Start date: 2007-07-25
End date: 2007-08-21
Lyrica
Indication: Musculoskeletal Pain
Lyrica
Indication: Arthralgia
Hydrochlorothiazide
Administration route: Oral
Indication: Hypertension
Start date: 2007-03-08
End date: 2007-08-29
ALL Other Therapeutic Products
Indication: Pain
Amitiza
Administration route: Oral
Adverse event in 58 year old female receiving Hydrochlorothiazide
Reported by a physician from United States on 2007-10-18
Patient: 58 year old female
Adverse reactions / side effects: Blood Urea Increased, Blood Potassium Increased, Nodal Rhythm, Blood Creatine Increased, Syncope, Bradycardia, Blood Pressure Decreased, Asthenia, Blood Glucose Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Atenolol
Dosage: 100 mg; daily
Diltiazem Hydrochloride
Dosage: 360 mg; every morning; 240 mg; at bedtime
Captopril
Dosage: 50 mg; twice a day
Hydrochlorothiazide
Adverse event in 51 year old male receiving Hydrochlorothiazide
Reported by a pharmacist from United States on 2007-10-18
Patient: 51 year old male
Adverse reactions / side effects: Syncope, Hypotension
Adverse event resulted in: hospitalization
Suspect drug(s):
Hydrochlorothiazide
Dosage: 25mg qd
Indication: Hypertension
Start date: 2007-07-29
End date: 2007-08-02
Imdur
Dosage: 30mg qd
Indication: Hypertension
Start date: 2007-07-29
End date: 2007-08-02
Labetalol HCL
Dosage: 300 mg bid
Indication: Hypertension
Start date: 2007-07-29
End date: 2007-08-02
Lisinopril
Dosage: 40 mg qd
Indication: Hypertension
Start date: 2007-07-29
End date: 2007-08-02
Other drugs received by patient: Amiodarone; Aspirin; Zetia; Zocor
Adverse event in 66 year old male receiving Hydrochlorothiazide
Reported by a pharmacist from United States on 2007-10-18
Patient: 66 year old male, weighing 64.5 kg (141.9 pounds)
Adverse reactions / side effects: Grand MAL Convulsion, Confusional State, Mouth Haemorrhage, Hyponatraemia
Adverse event resulted in: hospitalization
Suspect drug(s):
Hydrochlorothiazide
Other drugs received by patient: Nicotine; Lorazepam; Atenolol; Lisinopril; Nifedipine; Aspirin; Multi-Vitamin
Adverse event in 61 year old male receiving Hydrochlorothiazide
Reported by a physician from United States on 2007-10-18
Patient: 61 year old male
Adverse reactions / side effects: Blood Urea Increased, Nodal Rhythm, Disorientation, Blood Creatine Increased, Haemoglobin Decreased, Haematocrit Decreased, Sinus Arrest, Blood Pressure Decreased, Lethargy
Adverse event resulted in: hospitalization
Suspect drug(s):
Nadolol
Dosage: 40 mg; daily
Diltiazem Hydrochloride
Dosage: 300 mg; daily
Hydrochlorothiazide
Dosage: 32.5 mg; daily
Irbesartan
Dosage: 300 mg; daily
Adverse event in 60 year old male receiving Hydrochlorothiazide
Reported by a physician from United States on 2007-10-18
Patient: 60 year old male
Adverse reactions / side effects: Syncope
Suspect drug(s):
Metoprolol Tartrate
Dosage: 75 mg; twice a day; , 50 mg; daily;
Valsartan
Dosage: 160 mg; twice a day;
Hydrochlorothiazide
Dosage: 12.5 mg; twice a day;
Amlodipine Besylate
Dosage: 20 mg; daily;
Adverse event in male receiving Hydrochlorothiazide
Reported by a consumer/non-health professional from United States on 2007-10-17
Patient: male
Adverse reactions / side effects: Renal Disorder, Gastrooesophageal Reflux Disease, Tinea Pedis, Sunburn
Suspect drug(s):
Norvasc
Indication: Hypertension
Hydrochlorothiazide
Indication: Hypertension
Lisinopril
Indication: Hypertension
Adverse event in 67 year old female receiving Hydrochlorothiazide
Reported by a physician from Germany on 2007-10-17
Patient: 67 year old female
Adverse reactions / side effects: Rhabdomyolysis, Drug Interaction, Renal Failure Acute
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Vytorin
Administration route: Oral
Indication: Hyperlipidaemia
Start date: 2005-12-01
End date: 2006-01-01
Clonidine Hydrochloride
Indication: Hypertension
Indapamide
Administration route: Oral
Indication: Hypertension
Hydrochlorothiazide
Administration route: Oral
Indication: Hypertension
Hydrochlorothiazide and Losartan Potassium
Administration route: Oral
Indication: Hypertension
Allopurinol
Administration route: Oral
Meloxicam
Indication: Back Pain
Start date: 2006-01-02
Meloxicam
Indication: Abdominal Pain Lower
Start date: 2006-01-02
Acetaminophen and Codeine Phosphate
Administration route: Oral
Indication: Back Pain
Start date: 2006-01-02
Acetaminophen and Codeine Phosphate
Administration route: Oral
Indication: Abdominal Pain Lower
Start date: 2006-01-02
Pridinol Mesylate
Administration route: Oral
Indication: Back Pain
Start date: 2006-01-02
Pridinol Mesylate
Administration route: Oral
Indication: Abdominal Pain Lower
Start date: 2006-01-02
Dipyrone
Administration route: Oral
Indication: Back Pain
Start date: 2006-01-03
Dipyrone
Administration route: Oral
Indication: Abdominal Pain Lower
Start date: 2006-01-03
Esomeprazole Magnesium
Administration route: Oral
Indication: Gastric Disorder
Start date: 2006-01-04
Esomeprazole Magnesium
Administration route: Oral
Indication: Nausea
Start date: 2006-01-04
Metoclopramide Hydrochloride
Administration route: Oral
Indication: Gastric Disorder
Start date: 2006-01-04
Metoclopramide Hydrochloride
Administration route: Oral
Indication: Nausea
Start date: 2006-01-04
[therapy Unspecified]
Administration route: Oral
Indication: Gastric Disorder
Start date: 2006-01-04
[therapy Unspecified]
Administration route: Oral
Indication: Nausea
Start date: 2006-01-04
Other drugs received by patient: Lercanidipine Hydrochloride; Nebivolol Hydrochloride
Adverse event in female receiving Hydrochlorothiazide
Reported by a individual with unspecified qualification from United States on 2007-10-17
Patient: female, weighing 99.8 kg (219.5 pounds)
Adverse reactions / side effects: Pulmonary Hypertension, Diverticulum, Type 2 Diabetes Mellitus, Obesity, Hypothyroidism, Blood Cholesterol Increased, Blood Potassium Increased, Depression
Suspect drug(s):
Diovan
Dosage: 320mg, unk
Indication: Hypertension
Coreg
Dosage: 40mg, unk
Indication: Hypertension
Hydrochlorothiazide
Dosage: 25mg, unk
Indication: Hypertension
Potassium Chloride
Dosage: 40meq, unk
Indication: Hypertension
Other drugs received by patient: Fosamax; Toprol-XL; Torsemide; Caduet
Adverse event in 72 year old female receiving Hydrochlorothiazide
Reported by a individual with unspecified qualification from United Kingdom on 2007-10-17
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):
Lisinopril
Dosage: 20 mg/day
Administration route: Oral
Indication: Hypertension
Hydrochlorothiazide
Dosage: 12.5 mg/day
Administration route: Oral
Indication: Hypertension
Start date: 2007-03-03
Other drugs received by patient: Amlodipine; Atorvastatin Calcium; Lantus; Metformin HCL
Adverse event in female receiving Hydrochlorothiazide
Reported by a consumer/non-health professional from United States on 2007-10-16
Patient: female
Adverse reactions / side effects: Spinal Fusion Surgery, Blood Pressure Inadequately Controlled
Suspect drug(s):
Nifedipine
Administration route: Oral
Indication: Hypertension
Hydrochlorothiazide
Administration route: Oral
Indication: Hypertension
Start date: 1990-01-01
Lisinopril
Indication: Hypertension
Other drugs received by patient: Oxycontin; Motrin
Adverse event in female receiving Hydrochlorothiazide
Reported by a pharmacist from France on 2007-10-15
Patient: female
Adverse reactions / side effects: Confusional State, Hypersensitivity, Depersonalisation, Multiple Myeloma, Pyrexia, Hepatitis, Loss of Consciousness, Hypokinesia, Spinal Compression Fracture, Skin Lesion, Inappropriate Antidiuretic Hormone Secretion, Humerus Fracture, Back Pain, Phlebitis, Pain in Extremity, Musculoskeletal Pain, Hyponatraemia, Amnesia, Epilepsy, Spondylitis, Renal Failure, Respiratory Failure, Staphylococcal Infection, Sepsis, Blood Pressure Decreased
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Depakene
Administration route: Oral
Indication: Facial Neuralgia
Start date: 2004-10-18
End date: 2004-11-01
Hydrochlorothiazide
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 1999-01-01
End date: 2004-11-01
Other drugs received by patient: Amlodipine; Irbesartan; Omeprazole; Domperidone; Nitrofurantoin; Nifedipine
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