Hydrochlorothiazide 25mgtablets
Overview
What is this medicine?
How to Use This Medicine
To get the most benefit from your medication, follow your doctor's instructions carefully. Read all the information provided to you and follow the instructions closely.
Continuing Your Medication
Continue taking your medication as directed by your doctor or healthcare provider, even if you start to feel better. This medication may increase the frequency of urination, so try to avoid taking it too close to bedtime to minimize sleep disturbances.
Oral Suspension Instructions
You can take the oral suspension with or without food. Before using, shake the suspension well to ensure the medication is evenly mixed. Measure the liquid dose carefully using the measuring device provided with the medication. If a measuring device is not included, ask your pharmacist for one to ensure accurate dosing.
Storing and Disposing of Your Medication
Store all forms of this medication at room temperature, protected from light and moisture. Keep the medication in a dry place, away from the bathroom, and make sure the lid is tightly closed.
Missing a Dose
If you miss a dose, take it as soon as you remember. However, if it's close to the time for your next scheduled dose, skip the missed dose and resume your regular dosing schedule. Do not take two doses at the same time or take extra doses to make up for a missed dose.
Lifestyle & Tips
- Take the medication exactly as prescribed, usually once daily in the morning to avoid frequent urination at night.
- Do not stop taking the medication without consulting your doctor, even if you feel well.
- Follow a low-sodium diet as advised by your doctor or dietitian.
- Maintain regular physical activity as recommended.
- Limit alcohol intake, as it can worsen dizziness or lower blood pressure too much.
- Stay hydrated, but avoid excessive fluid intake unless advised by your doctor.
- Protect yourself from the sun (wear protective clothing, use sunscreen) as this medication can increase sun sensitivity.
Available Forms & Alternatives
Dosing & Administration
Adult Dosing
Condition-Specific Dosing:
Pediatric Dosing
Dose Adjustments
Renal Impairment:
Hepatic Impairment:
Pharmacology
Mechanism of Action
Pharmacokinetics
Absorption:
Distribution:
Elimination:
Pharmacodynamics
Safety & Warnings
Side Effects
Although rare, some people may experience severe and potentially life-threatening side effects while taking this medication. If you notice any of the following symptoms, contact your doctor or seek medical help right away:
Signs of an allergic reaction: rash, hives, itching, red, swollen, blistered, or peeling skin (with or without fever), wheezing, tightness in the chest or throat, trouble breathing, swallowing, or talking, unusual hoarseness, or swelling of the mouth, face, lips, tongue, or throat.
Signs of high blood sugar: confusion, drowsiness, unusual thirst or hunger, frequent urination, flushing, rapid breathing, or fruity-smelling breath.
Signs of fluid and electrolyte problems: mood changes, confusion, muscle pain or weakness, irregular heartbeat, severe dizziness or fainting, increased thirst, seizures, extreme fatigue or weakness, decreased appetite, difficulty urinating or changes in urine output, dry mouth, dry eyes, or severe nausea and vomiting.
Signs of pancreatitis (pancreas problems): severe abdominal pain, severe back pain, or severe nausea and vomiting.
Signs of kidney problems: difficulty urinating, changes in urine output, blood in the urine, or sudden weight gain. Additionally, dark urine or yellowing of the skin and eyes may occur.
Fever, chills, or sore throat; unexplained bruising or bleeding; or feeling extremely tired or weak.
Abnormal sensations such as burning, numbness, or tingling.
Shortness of breath.
Restlessness.
Difficulty achieving or maintaining an erection.
Eye Problems:
This medication can cause certain eye problems, which may lead to permanent vision loss if left untreated. If you experience eye problems, symptoms such as changes in vision or eye pain typically occur within hours to weeks of starting this medication. Contact your doctor immediately if you notice any of these signs.
Skin Cancer Risk:
Rarely, people taking hydrochlorothiazide have developed certain types of skin cancer. To minimize this risk, protect your skin from the sun and follow your doctor's recommendations for skin checks. If you notice any changes in the color or size of a mole, or any new or changing skin lump or growth, contact your doctor right away.
Other Side Effects:
Most people experience few or no side effects while taking this medication. However, some common side effects may occur, including:
Constipation, diarrhea, upset stomach, vomiting, or decreased appetite.
Stomach cramps.
Dizziness, fatigue, or weakness.
Headache.
If any of these side effects or other symptoms bother you or persist, contact your doctor or seek medical help.
Reporting Side Effects:
If you have questions or concerns about side effects, contact your doctor. You can also report side effects to the FDA at 1-800-332-1088 or online at https://www.fda.gov/medwatch.
Seek Immediate Medical Attention If You Experience:
- Severe dizziness or fainting
- Unusual tiredness or weakness
- Muscle cramps or spasms
- Irregular or fast heartbeat
- Extreme thirst or dry mouth
- Nausea or vomiting
- Confusion or mood changes
- Signs of allergic reaction (rash, hives, swelling of face/lips/tongue, difficulty breathing)
Before Using This Medicine
It is essential to inform your doctor about the following:
Any allergies you have, including allergies to this medication, its components, or other substances, such as foods or drugs. Be sure to describe the allergic reaction you experienced, including any symptoms that occurred.
A known sulfa allergy, as this may affect your ability to take this medication safely.
Any difficulties with urination, as this medication may not be suitable for individuals with urinary retention.
If you are currently taking dofetilide, as this combination may increase the risk of adverse interactions.
* If you are taking lithium, as this medication may interact with lithium and affect its efficacy or increase the risk of side effects.
This list is not exhaustive, and it is crucial to discuss all your medications, including prescription and over-the-counter drugs, natural products, and vitamins, with your doctor and pharmacist. They will help you determine whether it is safe to take this medication in conjunction with your other medications and health conditions. Never start, stop, or adjust the dosage of any medication without first consulting your doctor to ensure your safety.
Precautions & Cautions
To ensure your safety, avoid driving and other activities that require alertness until you understand how this medication affects you. When getting up from a sitting or lying down position, rise slowly to minimize the risk of dizziness or fainting. Be cautious when climbing stairs.
Regular blood work and laboratory tests are crucial, as directed by your doctor. This medication may cause elevated cholesterol and triglyceride levels. If you have a history of high cholesterol or triglycerides, consult your doctor.
If you have diabetes, closely monitor your blood sugar levels. Additionally, check your blood pressure as advised by your doctor. This medication may interfere with certain laboratory tests, so it is vital to inform all your healthcare providers and laboratory personnel that you are taking this medication.
If you have high blood pressure, consult your doctor before using over-the-counter products that may increase blood pressure, such as cough or cold medications, diet pills, stimulants, non-steroidal anti-inflammatory drugs (NSAIDs) like ibuprofen or naproxen, and certain natural products or aids.
As this medication is a potent diuretic, it may lead to excessive loss of water and electrolytes (like potassium) in the blood, resulting in severe health complications. Your doctor will closely monitor you to adjust the dosage according to your body's needs.
If you are on a low-sodium or sodium-free diet, discuss this with your doctor. Before consuming alcohol, marijuana, or other forms of cannabis, or taking prescription or over-the-counter medications that may cause drowsiness, consult your doctor.
Inform your doctor if you experience excessive sweating, fluid loss, vomiting, or diarrhea, as these may lead to low blood pressure. If you are taking cholestyramine or colestipol, consult your pharmacist about the proper administration of these medications with this drug. Be aware of the potential for gout attacks.
If you have lupus, this medication may exacerbate your condition. Immediately report any new or worsening symptoms to your doctor. This medication may increase your susceptibility to sunburn, so exercise caution when exposed to sunlight and inform your doctor if you experience unusual sunburn.
If you are 65 years or older, use this medication with caution, as you may be more prone to side effects. If you are pregnant, plan to become pregnant, or are breastfeeding, discuss the benefits and risks of this medication with your doctor.
Overdose Information
Overdose Symptoms:
- Dehydration
- Electrolyte imbalance (e.g., severe hypokalemia, hyponatremia)
- Hypotension (low blood pressure)
- Dizziness, weakness, confusion
- Nausea, vomiting
- Cardiac arrhythmias
What to Do:
Seek immediate medical attention. Call 911 or Poison Control at 1-800-222-1222. Treatment is supportive and symptomatic, focusing on correcting fluid and electrolyte imbalances.
Drug Interactions
Contraindicated Interactions
- Anuria
- Hypersensitivity to hydrochlorothiazide or other sulfonamide-derived drugs
Major Interactions
- Lithium (decreased renal clearance of lithium, increased risk of toxicity)
- Nonsteroidal Anti-inflammatory Drugs (NSAIDs) (reduced antihypertensive and diuretic effects, increased risk of renal impairment)
- Digoxin (hypokalemia induced by HCTZ can potentiate digoxin toxicity)
- Corticosteroids (increased risk of hypokalemia)
- Antidiabetic agents (reduced hypoglycemic effect of insulin and oral hypoglycemics)
- Cholestyramine, Colestipol (reduced absorption of hydrochlorothiazide)
Moderate Interactions
- Alcohol, Barbiturates, Opioids (additive orthostatic hypotension)
- Pressor Amines (e.g., norepinephrine) (possible decreased arterial responsiveness)
- Skeletal Muscle Relaxants, Nondepolarizing (e.g., tubocurarine) (possible increased responsiveness)
- Allopurinol (increased risk of hypersensitivity reactions to allopurinol)
- Amantadine (increased risk of amantadine toxicity)
- Calcium salts (increased serum calcium levels)
Minor Interactions
- Not available
Monitoring
Baseline Monitoring
Rationale: To establish baseline and assess efficacy.
Timing: Prior to initiation
Rationale: To establish baseline and identify pre-existing imbalances; HCTZ can cause hypokalemia, hyponatremia, hypomagnesemia, and hypercalcemia.
Timing: Prior to initiation
Rationale: To assess baseline kidney function and guide dosing; HCTZ is less effective in severe renal impairment.
Timing: Prior to initiation
Rationale: HCTZ can increase uric acid levels, potentially precipitating gout.
Timing: Prior to initiation
Rationale: HCTZ can cause hyperglycemia, especially in diabetic or pre-diabetic patients.
Timing: Prior to initiation
Routine Monitoring
Frequency: Regularly (e.g., weekly initially, then monthly or as clinically indicated)
Target: Individualized based on patient's condition (e.g., <130/80 mmHg for most adults)
Action Threshold: If BP remains uncontrolled or drops excessively (e.g., symptomatic hypotension), adjust dose or therapy.
Frequency: Initially within 1-2 weeks of initiation/dose change, then periodically (e.g., every 3-6 months or as clinically indicated), especially in patients at risk for imbalances (e.g., concomitant medications, vomiting/diarrhea).
Target: Sodium: 135-145 mEq/L; Potassium: 3.5-5.0 mEq/L; Magnesium: 1.7-2.2 mg/dL; Calcium: 8.5-10.2 mg/dL
Action Threshold: Significant deviations (e.g., K < 3.0 mEq/L, Na < 130 mEq/L) require intervention (e.g., supplementation, dose reduction, discontinuation).
Frequency: Periodically (e.g., every 3-6 months or as clinically indicated), especially in elderly or those with pre-existing renal impairment.
Target: Within normal limits for patient's age/baseline.
Action Threshold: Significant increase in creatinine (e.g., >30% from baseline) may indicate renal impairment and require dose adjustment or discontinuation.
Frequency: Periodically (e.g., every 3-6 months or as clinically indicated), especially in diabetic patients.
Target: Individualized based on patient's diabetic control.
Action Threshold: Persistent hyperglycemia may require adjustment of antidiabetic therapy or HCTZ discontinuation.
Frequency: Periodically (e.g., every 6-12 months or as clinically indicated), especially in patients with history of gout.
Target: Within normal limits or individualized for gout prevention.
Action Threshold: Symptomatic hyperuricemia or gout flares may require intervention.
Symptom Monitoring
- Dizziness or lightheadedness (especially when standing up)
- Muscle cramps or weakness
- Unusual thirst or dry mouth
- Nausea or vomiting
- Fatigue or lethargy
- Irregular heartbeat
- Swelling of ankles or feet (if edema is not resolving)
- Signs of allergic reaction (rash, itching, swelling)
Special Patient Groups
Pregnancy
Hydrochlorothiazide is generally not recommended for routine use during pregnancy, especially in the second and third trimesters (Pregnancy Category D). It can cause fetal or neonatal jaundice, thrombocytopenia, and other adverse reactions observed in adults. It should only be used if the potential benefit justifies the potential risk to the fetus.
Trimester-Specific Risks:
Lactation
Hydrochlorothiazide is excreted in breast milk. While generally considered compatible with caution (L3), it may decrease milk supply, especially in high doses or in mothers with compromised lactation. Monitor the infant for signs of dehydration, electrolyte imbalance, or jaundice.
Pediatric Use
Use with caution. Dosing is weight-based. Children may be more susceptible to electrolyte imbalances. Close monitoring of fluid and electrolytes is essential.
Geriatric Use
Elderly patients may be more sensitive to the effects of hydrochlorothiazide, particularly regarding electrolyte imbalances (e.g., hypokalemia, hyponatremia), dehydration, and orthostatic hypotension. Start with lower doses and titrate slowly. Close monitoring of fluid status, electrolytes, and renal function is crucial.
Clinical Information
Clinical Pearls
- Instruct patients to take hydrochlorothiazide in the morning to prevent nocturia (waking up to urinate at night).
- Monitor serum potassium levels closely, especially in patients on concomitant medications that can affect potassium (e.g., digoxin, corticosteroids) or those with pre-existing cardiac conditions.
- Advise patients about potential photosensitivity and recommend sun protection.
- Hydrochlorothiazide is generally less effective in patients with significant renal impairment (CrCl < 30 mL/min); a loop diuretic may be more appropriate in such cases.
- Can cause mild elevation in blood glucose, uric acid, and calcium levels, and decrease in potassium, sodium, and magnesium levels.
Alternative Therapies
- Loop diuretics (e.g., Furosemide, Torsemide) for more potent diuresis or in renal impairment
- Potassium-sparing diuretics (e.g., Spironolactone, Amiloride) for diuresis with potassium conservation
- Other classes of antihypertensives (e.g., ACE inhibitors, Angiotensin Receptor Blockers, Calcium Channel Blockers, Beta-blockers) for blood pressure control