Clinical data | |
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Pronunciation | meh-THEH-na-meen[1] |
Trade names | Antihydral, Hiprex, Urex, Urotropin, others |
Other names | Hexamethylenetetramine; HMTA; Hexamine; Hexamethylenamine; Hexamethyleneamine; Metenamine; Urometine; Hippramine; E-239; R-657; 1,3,5,7-Tetraazaadamantane |
Routes of administration | Oral,[2][3][4] topical[5][6] |
Drug class | Antiseptic; Antibacterial |
ATC code |
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Pharmacokinetic data | |
Bioavailability | High (≥70%)[7][8][2] |
Protein binding | Unknown[3] |
Metabolism | Hydrolysis in acidic urine[3] |
Metabolites | • Formaldehyde[3][9] • Ammonia[3][9] • Formic acid[10][11] |
Onset of action | ≤30 minutes[3][4] |
Elimination half-life | 2–6 hours[2][7][3] |
Excretion | Urine: 70–90% unchanged within 24 hours[3] |
Identifiers | |
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Chemical and physical data | |
Formula | C6H12N4 |
Molar mass | 140.190 g·mol−1 |
3D model (JSmol) | |
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Methenamine, also known as hexamine or hexamethylenetetramine and sold under the brand names Hiprex, Urex, and Urotropin among others, is a urinary tract antiseptic and antibacterial medication which is used in the prevention of recurrent urinary tract infections (UTIs).[4][3][1][8][12] It is not an antibiotic, and unlike antibiotics, has no risk of bacterial resistance.[9][13][8] Methenamine can reduce the risk of UTIs by 44 to 86% and has been found to be non-inferior to low-dose prophylactic antibiotics.[12][14][15] It is taken by mouth.[3][8] The drug is available both by prescription and at lower doses over the counter.[2][16][4][17] Besides for UTI prevention, methenamine is also available in a topical form to treat hyperhidrosis.[5][6][18]
Side effects of methenamine are generally minor and include upset stomach, nausea, and headache, among others.[3][19][7] Methenamine is a prodrug of formaldehyde in acidic urine.[3][8][9] Formaldehyde is a non-specific antiseptic and bactericide which works via denaturation of bacterial proteins and nucleic acids.[2][3][8][9] Conversion of methenamine into formaldehyde only occurs in acidic environments and hence its actions show selectivity for tissues like the bladder and stomach.[8][20] Chemically, methenamine is a simple cyclized hydrocarbon and is similar in structure to adamantane.[13][7][8]
Methenamine was discovered in 1859[7] and was first introduced for medical use as a urinary antiseptic in 1895.[21][22] It was formally approved for medical use in the United States in 1967.[23] Though it became a "forgotten drug" following the discovery of antibiotics in 1928, there has been a resurgence in interest in methenamine since 2010 owing to increasing rates of bacterial resistance with antibiotics.[2][8][7][14][24] Larger and higher-quality clinical trials of methenamine for UTI prevention have started to be published in the 2020s and it may soon be recommended by more medical guidelines.[2][14][19][25][15] Methenamine has been found to be more cost-effective than low-dose prophylactic antibiotics for preventing UTIs.[26]
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