Methenamine/sodium biphosphate Disease Interactions
There are 8 disease interactions with methenamine / sodium biphosphate.
- Inflammatory bowel disease
- Intestinal obstruction disorders
- Crystalluria
- Gout
- Liver disease
- Hypocalcemia
- Phosphate imbalance
- Electrolyte imbalance
Laxatives (applies to methenamine/sodium biphosphate) inflammatory bowel disease
Major Potential Hazard, Moderate plausibility.
The use of laxatives is contraindicated in patients with inflammatory bowel disease. Patients with inflammatory bowel disease may experience colonic perforation with use of stimulant laxatives.
References (6)
- (2001) "Product Information. Dulcolax (bisacodyl)." Ciba Self-Medication Inc
- "Product Information. Fleet Bisacodyl (bisacodyl)." Fleet
- "Product Information. Kondremul Plain (mineral oil)." Bristol-Myers Squibb
- (2001) "Product Information. Neoloid (castor oil)." Paddock Laboratories Inc
- (2022) "Product Information. SenoSol-X (senna)." Apothecon Inc
- (2010) "Product Information. Suprep Bowel Prep Kit (magnesium/potassium/sodium sulfates)." Braintree Laboratories
Laxatives (applies to methenamine/sodium biphosphate) intestinal obstruction disorders
Major Potential Hazard, Moderate plausibility. Applicable conditions: Gastrointestinal Obstruction
The use of laxatives is contraindicated in patients with intestinal obstruction disorders. Patients with intestinal obstruction disorders may need their underlying condition treated to correct the constipation. Some laxatives require reduction in the colon to their active form to be effective which may be a problem in patients with intestinal obstruction.
References (8)
- (2001) "Product Information. Dulcolax (bisacodyl)." Ciba Self-Medication Inc
- "Product Information. Fleet Bisacodyl (bisacodyl)." Fleet
- "Product Information. Kondremul Plain (mineral oil)." Bristol-Myers Squibb
- (2001) "Product Information. Fleet Mineral Oil Enema (mineral oil)." Fleet
- (2001) "Product Information. Citrucel (methylcellulose)." SmithKline Beecham
- (2001) "Product Information. Fleet Babylax (glycerin)." Alcon Laboratories Inc
- (2022) "Product Information. SenoSol-X (senna)." Apothecon Inc
- (2010) "Product Information. Suprep Bowel Prep Kit (magnesium/potassium/sodium sulfates)." Braintree Laboratories
Methenamine (applies to methenamine/sodium biphosphate) crystalluria
Major Potential Hazard, High plausibility. Applicable conditions: Renal Dysfunction, Dehydration
The use of methenamine salts (i.e. methenamine hippurate or mandelate), but not the base, is contraindicated in patients with severe renal impairment or dehydration. Methenamine is excreted by the kidney and concentrated in the urine. In patients with low urinary output, the salts can precipitate and cause crystalluria.
References (6)
- Klinge E, Mannisto P, Mantyla R, Lamminsivu U, Ottoila P (1982) "Pharmacokinetics of methenamine in healthy volunteers." J Antimicrob Chemother, 9, p. 209-16
- Gleckman R, Alvarez S, Joubert D, Matthews S (1979) "Drug therapy reviews: methenamine mandelate and methenamine hippurate." Am J Hosp Pharm, 36, p. 1509-12
- Australian Drug Evaluation Committee (1972) "Adverse effects of drugs commonly used in the treatment of urinary tract infection." Med J Aust, 1, p. 435-8
- (2002) "Product Information. Hiprex (methenamine)." Hoechst Marion Roussel
- (2002) "Product Information. Mandelamine (methenamine)." Parke-Davis
- American Medical Association, Division of Drugs and Toxicology (1994) "Drug evaluations annual 1994." Chicago, IL: American Medical Association;
Methenamine (applies to methenamine/sodium biphosphate) gout
Major Potential Hazard, Moderate plausibility.
Methenamine mandelate (salts), should be avoided in patients with gout as it may precipitate urate crystals in their urine. A similar situation may arise in patients with a predisposition to the formation of uric acid stones.
References (1)
- (2002) "Product Information. Hiprex (methenamine)." Hoechst Marion Roussel
Methenamine (applies to methenamine/sodium biphosphate) liver disease
Major Potential Hazard, High plausibility.
The use of methenamine and its salts (i.e. methenamine hippurate or mandelate) is contraindicated in patients with severe hepatic impairment. Methenamine is hydrolyzed to ammonia and formaldehyde in the urine under acidic conditions. Patients with liver disease may already have elevated ammonia levels, which can cause or exacerbate hepatic encephalopathy. Methenamine hippurate has also been associated with isolated cases of transient elevations in serum transaminases. The manufacturer recommends periodic liver function tests during therapy, particularly in patients with preexisting liver dysfunction.
References (5)
- Strom J, Jun H (1975) "Kinetics of hydrolysis of methenamine." Pharm Bull, 23, p. 651
- Gleckman R, Alvarez S, Joubert D, Matthews S (1979) "Drug therapy reviews: methenamine mandelate and methenamine hippurate." Am J Hosp Pharm, 36, p. 1509-12
- (2002) "Product Information. Hiprex (methenamine)." Hoechst Marion Roussel
- (2002) "Product Information. Mandelamine (methenamine)." Parke-Davis
- American Medical Association, Division of Drugs and Toxicology (1994) "Drug evaluations annual 1994." Chicago, IL: American Medical Association;
Phosphates (applies to methenamine/sodium biphosphate) hypocalcemia
Major Potential Hazard, High plausibility. Applicable conditions: Pancreatitis
The use of phosphates is in general contraindicated in conditions where high potassium, high phosphate, or low calcium may be encountered such as hypoparathyroidism, osteomalacia, acute pancreatitis, or chronic renal disease.
References (2)
- (2001) "Product Information. K-Phos Neutral (potassium phosphate)." Beach Pharmaceuticals
- (2001) "Product Information. Fleet Enema (sodium acid phosphate-sodium phosphate)." Fleet
Phosphates (applies to methenamine/sodium biphosphate) phosphate imbalance
Major Potential Hazard, High plausibility. Applicable conditions: Hypoparathyroidism, Renal Dysfunction
Therapy with phosphates should be administered with extreme caution in patients with hyperphosphatemia (hypoparathyroidism or severe renal impairment). Elevated serum concentrations of phosphate and calcium can exceed the solubility level and result in calcium-phosphate precipitates that deposit in vascular and renal systems as well as other soft tissues of the body. Clinical monitoring of serum calcium and phosphate concentrations is necessary.
References (2)
- (2001) "Product Information. K-Phos Neutral (potassium phosphate)." Beach Pharmaceuticals
- (2001) "Product Information. Fleet Enema (sodium acid phosphate-sodium phosphate)." Fleet
Sodium phosphate (applies to methenamine/sodium biphosphate) electrolyte imbalance
Major Potential Hazard, High plausibility. Applicable conditions: Dehydration, Congestive Heart Failure, Phosphate Imbalance, Gastrointestinal Obstruction, Inflammatory Bowel Disease
The use of sodium phosphates is contraindicated in patients with congenital megacolon, intestinal obstruction, imperforate anus, active inflammatory disease or congestive heart failure. Serious, potentially life-threatening electrolyte imbalance such as hypocalcemia and hyperphosphatemia can result with prolonged or excessive use of phosphate laxatives. Hypernatremia and dehydration can occur due to improper dilution of hypertonic saline laxatives. Therapy with sodium phosphates should be administered cautiously and frequency of administration limited in patients with renal dysfunction, colostomy, cardiac dysfunction, or electrolyte imbalance. Clinical monitoring of electrolyte concentrations is recommended.
References (2)
- (2001) "Product Information. Magnesium Sulfate (magnesium sulfate)." Abbott Pharmaceutical
- (2001) "Product Information. Fleet Enema (sodium acid phosphate-sodium phosphate)." Fleet
Switch to consumer interaction data
Methenamine/sodium biphosphate drug interactions
There are 449 drug interactions with methenamine / sodium biphosphate.
Methenamine/sodium biphosphate alcohol/food interactions
There is 1 alcohol/food interaction with methenamine / sodium biphosphate.
Drug Interaction Classification
Highly clinically significant. Avoid combinations; the risk of the interaction outweighs the benefit. | |
Moderately clinically significant. Usually avoid combinations; use it only under special circumstances. | |
Minimally clinically significant. Minimize risk; assess risk and consider an alternative drug, take steps to circumvent the interaction risk and/or institute a monitoring plan. | |
No interaction information available. |
Further information
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