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cimetidine (Tagamet HB)

 

Classes: Histamine H2 Antagonists

Dosing and uses of Tagamet HB (cimetidine)

 

Adult dosage forms and strengths

injectable solution

  • 150mg/mL

oral solution

  • 300mg/5mL

tablet

  • 200mg
  • 300mg
  • 400mg (Rx)
  • 600mg (Rx)
  • 800mg (Rx)

 

Benign Gastric Ulcer

800 mg PO qHS Or

400 mg PO q12hr Or

300 mg PO q6hr

 

Duodenal Ulcer

800 mg PO qHS Or

400 mg PO q12hr Or

300 mg PO q6hr

 

Erosive Gastroesophageal Reflux Disease

800 mg PO q12hr Or

400 mg PO q6hr

 

Heartburn

Over the counter only

To relieve symptoms: 200 mg PO up to q12hr

To prevent symptoms: 200 mg PO with glass of water right before or any time up to 30 minutes before eating food or drinking beverages that cause heartburn

 

Pathological Hypersecretory Conditions

300 mg PO q6hr with meals and Hs

 

Renal Impairment

CrCl<30 mL/min

300 mg IV/IO q12hr

Prevention of upper GI bleeding: 25 mg/hour continuous IV infusion

 

Other Indications & Uses

PUD (treatment, maintenance), gastric ulcer treatment, GI bleeding prevention in critically ill patients, hypersecretory conditions (e.g., Zollinger-Ellison)

 

Pediatric dosage forms and strengths

injectable solution

  • 150mg/mL

oral solution

  • 300mg/5mL

tablet

  • 200mg
  • 300mg
  • 400mg (Rx)
  • 600mg (Rx)
  • 800mg (Rx)

 

Duodenal Ulcer (Off-label)

<16 years: Use only if benefit outweighs risks

20-40 mg/kg/day IV/PO divided q6hr

Neonates (<28 days old): 5-20 mg/kg/day IV/PO divided q8-12hr

Infants: 10-20 mg/kg/day IV/PO divided q6-12hr

 

Geriatric dosage forms and strengths

Not drug of choice in elderly because of increased potential for confusion and drug interactions

 

Benign Gastric Ulcer

800 mg PO qHS Or

400 mg PO q12hr Or

300 mg PO q6hr

 

Duodenal Ulcer

800 mg PO qHS Or

400 mg PO q12hr Or

300 mg PO q6hr

 

Erosive Gastroesophageal Reflux Disease

800 mg PO q12hr Or

400 mg PO q6hr

 

Tagamet HB (cimetidine) adverse (side) effects

1-10%

Headache (2.1%)

Dizziness (1%)

Somnolence (1%)

Gynecomastia (0.3-4%)

 

Frequency not defined

Confusion (elderly)

Impotence

Diarrhea

Nausea

Vomiting

 

Warnings

Contraindications

Hypersensitivity to cimetidine or other H2 receptor antagonists

 

Cautions

Antiandrogen: may cause feminization & sexual dysfunction in males

 

Pregnancy and lactation

Pregnancy category: B

Lactation: enters breast milk/not recommended

 

Pregnancy categories

A: Generally acceptable. Controlled studies in pregnant women show no evidence of fetal risk.

B: May be acceptable. Either animal studies show no risk but human studies not available or animal studies showed minor risks and human studies done and showed no risk.

C: Use with caution if benefits outweigh risks. Animal studies show risk and human studies not available or neither animal nor human studies done.

D: Use in LIFE-THREATENING emergencies when no safer drug available. Positive evidence of human fetal risk.

X: Do not use in pregnancy. Risks involved outweigh potential benefits. Safer alternatives exist.

NA: Information not available.

 

Pharmacology of Tagamet HB (cimetidine)

Mechanism of action

H2-receptor antagonist; blocks H2-receptors of gastric parietal cells, leading to inhibition of gastric secretions

 

Pharmacokinetics

Bioavailability: PO: 60-70% (undergoes minimal 1st pass metabolism)

Protein Bound: 15-20%

Metabolism: Liver, inhibit microsomal enzymes

Metabolites: Cimetidine sulfoxide, 5-hydroxymethyl derivative (inactive met)

Dialyzable: Yes, removed by HD and Pd

Enzymes inhibited: hepatic CYP1A2, CYP2D6, CYP3A4

Half-Life

  • Adults: 2 hr; increases to 4-5 hr with renal impairment
  • Infant: 2.1-3.6 hr

Onset

  • IV: 30 min
  • PO: <1 hr

Duration

  • IV/IM: 4-5 hr
  • PO: 4-8 hr

Peak Plasma Time

  • IM: 15 min
  • PO: 45-90 min

Vd

  • Adults: 1 L/kg
  • Children 1-12 years: 2.13 L/kg

Clearance

  • Total Body: 30-48 L/hr
  • Renal: 13.8-30 L/hr (removed by HD & PD)

Excretion

  • Urine: 48-75%
  • Feces: 2-3% (<2% in bile)

 

Administration

IV/IM Administration

Administered IM with no dilution, Or

Slow direct IV injection over 5 min or more after dilution to a total of 20 mL with compatible diluent (NS), Or

Intermittent IV infusion over 15 to 20 min in at least 50 mL of compatible diluent, Or

Continuous IV infusion in 100 to 1000 mL of compatible diluent over 24 hr

 

IV Compatibilities

Additive: cefazolin, clindamycin, epinephrine, erythromycin, furosemide, gentamicin, lidocaine, norepinephrine, KCl, vancomycin, verapamil, vit B/C

Syringe: atropine, heparin

Y-site: esmolol, heparin

Not spec: carbenicillin, tetracycline

 

IV Incompatibilities

Additive: amphotericin B

Syringe: cefazolin, pentobarbital, atropine/pentobarbital, chlorpromazine, heparin (?), secobarbitaL

Y-site: allopurinol, amphotericin B, amsacrine, cefepime, indomethacin, warfarin

 

IV Preparation

Solution

  • Injections: in 5% sodium bicarbonate injection, NS, D5W, D10W or LR to a volume of 20 mL
  • Infusions: 300 mg in 100 mL D5W