What are the brand and generic names, dosage forms, pharmacologic categories, FDA-approved indications, dosage and frequency, mechanism of action, contraindications, adverse effects, and drug interactions for Hydrochlorothiazide (hydrochlorothiazide), Premarin (conjugated estrogens), and Risperdal (risperidone)?

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Hydrochlorothiazide, Premarin, and Risperdal: Drug Information Guide

Hydrochlorothiazide (HCTZ)

a. Brand and Generic Name

  • Generic name: Hydrochlorothiazide
  • Brand names: Microzide, HydroDIURIL, various combination products

b. Dosage Forms

  • Tablets: 12.5 mg, 25 mg, 50 mg

c. Pharmacologic Category

  • Thiazide diuretic

d. FDA-Approved Indications

  • Hypertension (alone or in combination with other antihypertensives)
  • Edema associated with congestive heart failure, hepatic cirrhosis, and corticosteroid/estrogen therapy

e. Dosage and Frequency

  • Hypertension: 12.5-50 mg once daily 1
  • Edema: 25-100 mg daily in single or divided doses

f. Mechanism of Action

  • Inhibits sodium and chloride reabsorption in the distal convoluted tubule, increasing excretion of sodium, chloride, water, potassium, and bicarbonate

g. Contraindications

  • Anuria
  • Hypersensitivity to sulfonamide-derived drugs
  • Severe renal dysfunction

h. Adverse Effects

  • Hypokalemia 2
  • Hypomagnesemia 2
  • Hyperuricemia
  • Hyperglycemia
  • Hyperlipidemia
  • Hypercalcemia
  • Photosensitivity

i. Drug Interactions

  • Dofetilide (contraindicated) 2
  • NSAIDs (decreased diuretic efficacy)
  • Lithium (increased lithium levels)
  • Digoxin (increased risk of digitalis toxicity due to hypokalemia)
  • Antidiabetic agents (may require dose adjustment due to hyperglycemic effect)

j. Patient Counseling Points

  • Take in the morning to prevent nighttime urination
  • Monitor for signs of electrolyte imbalance (muscle weakness, cramps)
  • May cause photosensitivity; use sun protection
  • May increase blood glucose; diabetic patients should monitor glucose levels
  • Report dizziness upon standing (orthostatic hypotension)

Premarin (Conjugated Estrogens)

a. Brand and Generic Name

  • Brand name: Premarin
  • Generic name: Conjugated estrogens

b. Dosage Forms

  • Tablets: 0.3 mg, 0.45 mg, 0.625 mg, 0.9 mg, and 1.25 mg 3

c. Pharmacologic Category

  • Estrogen hormone

d. FDA-Approved Indications

  • Treatment of moderate to severe vasomotor symptoms associated with menopause
  • Treatment of moderate to severe vulvar and vaginal atrophy associated with menopause
  • Prevention of postmenopausal osteoporosis
  • Treatment of hypoestrogenism due to hypogonadism, castration, or primary ovarian failure
  • Palliative treatment of metastatic breast cancer in select men and postmenopausal women
  • Palliative treatment of advanced androgen-dependent prostate cancer

e. Dosage and Frequency

  • Menopausal symptoms: 0.3-1.25 mg daily
  • Osteoporosis prevention: 0.3-0.625 mg daily
  • Hypogonadism: 0.3-0.625 mg daily cyclically
  • Advanced prostate cancer: 1.25-2.5 mg three times daily

f. Mechanism of Action

  • Binds to nuclear estrogen receptors in estrogen-responsive tissues
  • Increases synthesis of DNA, RNA, and proteins in target tissues
  • Reduces release of gonadotropin-releasing hormone from hypothalamus

g. Contraindications

  • Undiagnosed abnormal genital bleeding
  • Known or suspected estrogen-dependent neoplasia
  • Active or history of venous thromboembolism
  • Active or recent arterial thromboembolic disease
  • Liver dysfunction or disease
  • Known protein C, protein S, or antithrombin deficiency
  • Pregnancy

h. Adverse Effects

  • Increased risk of endometrial cancer (when used without progestin)
  • Increased risk of breast cancer
  • Venous thromboembolism
  • Stroke
  • Coronary heart disease
  • Gallbladder disease
  • Nausea, vomiting
  • Headache
  • Weight changes

i. Drug Interactions

  • CYP3A4 inducers (decreased estrogen effect)
  • CYP3A4 inhibitors (increased estrogen effect)
  • Thyroid replacement therapy (may require dose adjustment)
  • Anticoagulants (altered anticoagulant effect)

j. Patient Counseling Points

  • Use lowest effective dose for shortest duration
  • Report abnormal vaginal bleeding immediately
  • Increased risk of cardiovascular events and breast cancer
  • Regular breast examinations and mammograms recommended
  • Discontinue if jaundice, visual disturbances, or migraine occurs
  • May affect laboratory test results

Risperdal (Risperidone)

a. Brand and Generic Name

  • Brand name: Risperdal
  • Generic name: Risperidone

b. Dosage Forms

  • Tablets: 0.25 mg, 0.5 mg, 1 mg, 2 mg, 3 mg, 4 mg 4
  • Oral solution: 1 mg/mL
  • Orally disintegrating tablets: 0.5 mg, 1 mg, 2 mg, 3 mg, 4 mg
  • Long-acting injection: 12.5 mg, 25 mg, 37.5 mg, 50 mg

c. Pharmacologic Category

  • Atypical antipsychotic

d. FDA-Approved Indications

  • Schizophrenia in adults and adolescents (13-17 years)
  • Bipolar I disorder (manic or mixed episodes) in adults and children (10-17 years)
  • Irritability associated with autistic disorder in children and adolescents (5-16 years)

e. Dosage and Frequency

  • Schizophrenia (adults): Initial 1 mg twice daily, target dose 4-8 mg/day
  • Schizophrenia (adolescents): Initial 0.5 mg once daily, target dose 3 mg/day
  • Bipolar mania (adults): Initial 2-3 mg once daily, range 1-6 mg/day
  • Bipolar mania (children/adolescents): Initial 0.5 mg once daily, target dose 2.5 mg/day
  • Autism irritability: Initial 0.25 mg/day (< 20 kg) or 0.5 mg/day (≥ 20 kg), target dose 0.5-3 mg/day

f. Mechanism of Action

  • Antagonist at dopamine D2 and serotonin 5-HT2A receptors 5, 6
  • Also antagonizes alpha1 and alpha2 adrenergic receptors and H1 histamine receptors
  • The combination of D2 and 5-HT2A antagonism is believed to improve both positive and negative symptoms of schizophrenia with reduced extrapyramidal effects

g. Contraindications

  • Hypersensitivity to risperidone or any component of the formulation

h. Adverse Effects

  • Extrapyramidal symptoms (dose-dependent) 2
  • Weight gain
  • Hyperglycemia and diabetes mellitus
  • Hyperprolactinemia
  • QT interval prolongation
  • Orthostatic hypotension
  • Sedation
  • Tardive dyskinesia (with long-term use) 4
  • Neuroleptic malignant syndrome (rare)

i. Drug Interactions

  • CYP2D6 inhibitors (increased risperidone levels)
  • Carbamazepine and other CYP3A4 inducers (decreased risperidone levels)
  • Drugs that prolong QT interval (additive effect)
  • CNS depressants including alcohol (enhanced CNS depression) 4
  • Levodopa and dopamine agonists (antagonistic effect)

j. Patient Counseling Points

  • Take as prescribed, do not adjust dose without consulting healthcare provider
  • May cause orthostatic hypotension; rise slowly from sitting or lying position 4
  • May impair judgment, thinking, or motor skills; use caution when operating machinery 4
  • Report signs of high blood sugar (increased thirst, urination, hunger)
  • Avoid alcohol while taking risperidone 4
  • Use caution in hot weather and during exercise (risk of overheating)
  • Report involuntary muscle movements immediately
  • For women of childbearing potential, discuss pregnancy plans with healthcare provider 4

References

Guideline

Hypertension Management

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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