Trimethoprim (Alprim) - Uses, Dose, Side effects, MOA, Brands

Trimethoprim (Alprim) is an antibiotic that acts by inhibiting bacterial folate activation to tetrahydrofolate inhibiting bacterial protein and nucleic acid synthesis. It is used in the treatment of acute urinary tract infection, otitis media, and pneumocystis pneumonia infection.

Trimethoprim Uses:

  • Treatment of uncomplicated acute Cystitis (tablets, oral solution):

    • It is indicated for the treatment of simple urinary tract infections brought on by strains of the following organisms that are susceptible to it.:
      • Escherichia coli,
      • Proteus mirabilis,
      • Klebsiella pneumoniae,
      • Enterobacter species and
      • coagulase-negative Staphylococcus species, including S. saprophyticus.
  • Acute Otitis media (oral solution):

    • It is used to treat acute otitis media in children brought on by Haemophilus influenzae and susceptible strains of Streptococcus pneumoniae.
  • Off Label Use of Trimethoprim in Adults:

    • Acne vulgaris;
    • Treatment of mild to moderately severe pneumocystis pneumonia infection;
    • Prophylaxis of urinary tract infection.

Trimethoprim (Alprim) Dose in Adults

Trimethoprim (Alprim) Dose in the treatment of treatment of acute uncomplicated Cystitis:

  • For three days, take 100 mg twice a day.
  • Manufacturer's labeling:

    • 200 mg once a day (The dosing mentioned here may not reflect the current practice guidelines).

Trimethoprim (Alprim) Dose in the treatment of Acne vulgaris as an alternative therapy (off-label):

  • 100 mg orally thrice daily or 300 mg two times a day.
  • Treatment should be given for the shortest possible time to minimize bacterial resistance. Patients must be evaluated every three to four months.

Trimethoprim (Alprim) Dose as an alternative agent in the treatment of mild to moderate Pneumocystis pneumonia (off-label use):

  • Oral: 15 mg/kg/day in three divided doses in combination with dapsone for 21 days.

Trimethoprim (Alprim) Dose for the prophylaxis of uncomplicated Urinary tract infection (off-label):

  • 100 mg orally once a day.

Trimethoprim (Alprim) Dose in Children

Trimethoprim (Alprim) Dose in the treatment of acute Otitis media:

  • Infants ≥6 months, Children, and Adolescents:

    • For ten days, take 10 mg/kg/day orally in two divided doses at intervals of 12 hours.
    • The daily dosage cap is 400 mg.

Trimethoprim (Alprim) Dose in the treatment of uncomplicated urinary tract infection:

  • Infants ≥2 months, Children, and Adolescents:

Trimethoprim (Alprim) Dose in the treatment of Pneumocystis jirovecii pneumonia (PCP):

  • Children and Adolescents:

    • 15 mg/kg/day orally in three divided doses in combination with dapsone for 21 days.
    • Data in children is limited. The combination product, sulfamethoxazole and trimethoprim is preferred.

Pregnancy Risk Factor C

  • It may cross the placental boundary. It can cause adverse fetal outcomes due to its effect on folate metabolism.
  • Also, read the sulfamethoxazole/trimethoprim monograph for details

Trimethoprim use during breastfeeding:

  • Breast milk contains the drug, and its concentration is identical in maternal blood and breastmilk.
  • Breastmilk can contain antibiotics which may cause side effects, such as diarrhea and oral thrush.
  • It can also interfere with folate metabolism and is not recommended for breastfeeding.
  • Products that do not contain the combination (trimethoprim) are compatible with breastfeeding.
  • Also, read septran.

Dose in Kidney Disease:

  • Manufacturer's labeling:

    • CrCl >30 mL/minute: Use with caution, however, no dosage adjustment is necessary.
    • CrCl 15 to 30 mL/minute: Administer half of the recommended dose.
    • CrCl <15 mL/minute: Avoid in advanced renal disease.
  • Alternate recommendations:

    • Aronoff 2007: Note: Dose adjustments mentioned here are based on the usual daily dose of 100 mg twice a day.
      • CrCl >30 mL/minute: No dosage adjustment necessary.
      • CrCl 10 to 30 mL/minute: 100 mg administered every 18 hours.
    • CrCl <10 mL/minute: 100 mg once a day.
    • Intermittent Hemodialysis: It is 20% to 59% dialyzable. Administration of the dose after dialysis is recommended.
    • Peritoneal dialysis: 100 mg once a day.
  • HHS (OI adult 2019):

    • Treatment of Pneumocystis pneumonia:
      • Note: Dosage adjustments mentioned here are based on the usual maintenance dose of 5 mg/kg administered every 8 hours. Renal function may be estimated using the Cockcroft-Gault formula for dosage adjustment purposes.
      • CrCl >30 mL/minute: No dosage adjustment necessary.
      • CrCl 10 to 30 mL/minute: 5 mg/kg twice daily.
      • CrCl <10 mL/minute: 5 mg/kg once daily.
      • Intermittent Hemodialysis:
        • It is moderately dialyzable, about 20% to 59%.
        • Once daily at 5 mg/kg. On the day of the dialysis, the dose is given after hemodialysis.

Dose in Liver disease:

The manufacturer's labelling does not mention dosage modifications. In people with liver illness, it should be used cautiously.

Side effects of Trimethoprim (Alprim):

  • Dermatologic:

    • Maculopapular Rash
    • Phototoxicity
    • Pruritus
  • Endocrine & Metabolic:

    • Hyperkalemia
    • Hyponatremia
  • Gastrointestinal:

    • Epigastric Distress
    • Glossitis
    • Nausea
    • Vomiting
  • Hematologic & Oncologic:

    • Leukopenia
    • Megaloblastic Anemia
    • Methemoglobinemia
    • Neutropenia
    • Thrombocytopenia
  • Hepatic:

    • Increased Liver Enzymes
  • Hypersensitivity:

    • Anaphylaxis
    • Hypersensitivity Reaction
  • Renal:

    • Increased Blood Urea Nitrogen
    • Increased Serum Creatinine
  • Miscellaneous:

    • Fever

Contraindications to Trimethoprim (Alprim):

  • Allergy reactions to trimethoprim and any component of the formulation
  • Megaloblastic anemia due to folate deficiency

Warnings and precautions

  • Hematologic effects

    • High doses of medication or prolonged treatment may cause cytopenias, bone marrow suppression, and even death.
    • Patients on long-term therapy should be closely watched for indications of bone tumour suppression.
  • Hyperkalemia:

    • Treatment may result in hyperkalemia. Hyperkalemia is a risk for patients who are:
      • High doses (above 20 mg/kg/day)
      • Patients with severe renal impairment
      • Ageing is a good thing
      • Hypoaldosteronism is a form of and
      • Patients taking concomitant medication that can cause or exacerbate hyperkalemia.
  • Hypersensitivity

    • Rarely, severe allergic reactions can occur.
  • Superinfection

    • Long-term use can lead to superinfections, including fungal or bacterial infections.
    • Patients receiving long-term treatment may experience pseudomembranous colitis and C. difficile-associated diarrhea. 
    • This may occur up to two months after the last treatment.
  • Hepatic impairment

    • Patients with hepatic impairment need to be cautious.
  • Renal impairment

    • Patients with impaired renal function need to use it with caution.

Trimethoprim: Drug Interaction

Risk Factor C (Monitor therapy)

Alpelisib

May lower the serum level of CYP2C9 substrates (High risk with Inducers).

Amantadine

Trimethoprim might make Amantadine's harmful or hazardous effects worse. Particularly, there may be a higher chance of myoclonus and/or delirium.

Angiotensin II Receptor Blockers

Trimethoprim's serum levels may rise when amantadine is used. Trimethoprim may raise the level of amantadine in the blood. Angiotensin II Receptor Blockers' hyperkalemic impact may be increased by trimethoprim.

Angiotensin-Converting Enzyme Inhibitors

Angiotensin-Converting Enzyme Inhibitors' hyperkalemic impact may be enhanced by trimethoprim.

AzaTHIOprine

Azathioprine's myelosuppressive action may be strengthened by trimethoprim.

BCG Vaccine (Immunization)

Antibiotics may reduce the BCG vaccine's therapeutic effect (Immunization).

CYP2C9 Inhibitors (Moderate)

May slow down CYP2C9 substrate metabolism (High risk with Inhibitors).

Dapsone (Systemic)

The serum concentration of Dapsone may increase when taking trimethoprim (Systemic). The serum concentration of Trimethoprim may rise when Dapsone (Systemic) is used.

Dapsone (Topical)

Trimethoprim may intensify Dapsone's harmful or hazardous effects (Topical).More particular, trimethoprim might make hemolysis more likely.

Digoxin

The serum levels of Digoxin may rise when taking trimethoprim.

Eplerenone

Eplerenone's hyperkalemic impact may be enhanced by trimethoprim.

Lactobacillus and Estriol

The therapeutic effects of Lactobacillus and Estriol may be reduced by antibiotics.

LamiVUDine

LamiVUDine's serum concentration may be raised by trimethoprim.

Lumacaftor

May lower the serum level of CYP2C9 substrates (High Risk with Inhibitors or Inducers). The serum concentration of CYP2C9 Substrates may rise when taking lumacaftor (High Risk with Inhibitors or Inducers).

Memantine

Trimethoprim may intensify Memantine's harmful or hazardous effects. Particularly, there may be a higher chance of myoclonus and/or delirium. Memantine's serum levels may rise in response to trimethoprim. Trimethoprim's serum concentration could rise as a result of memantine.

Mercaptopurine

Mercaptopurine's myelosuppressive action may be strengthened by trimethoprim.

MetFORMIN

The serum concentration of MetFORMIN may rise when taking trimethoprim.

PRALAtrexate

Trimethoprim may raise PRALAtrexate's serum levels. More specifically, trimethoprim may lessen pralatrexate excretion. Management: Keep a close eye out for elevated pralatrexate serum levels and/or potential toxicity when trimethoprim is also being used. When stopping trimethoprim, keep an eye out for dropping pralatrexate levels.

Pyrimethamine

May intensify Trimethoprim's negative or hazardous effects.

Repaglinide

The metabolism of Repaglinide may be slowed down by trimethoprim.

RifAMPin

May lower the level of trimethoprim in the serum.

Rifapentine

May lower the serum level of CYP2C9 substrates (High risk with Inducers).

Spironolactone

Spironolactone's hyperkalemic impact may be enhanced by trimethoprim.

Thiazolidinediones

Thiazolidinediones may have reduced metabolism due to trimethoprim.

Varenicline

May lower the serum level of CYP2C9 substrates (High risk with Inducers). Management: When possible, look for CYP2C9 substrate substitutes. If concurrent therapy cannot be avoided, pay special attention to the substrate's clinical consequences (particularly therapeutic effects).

Risk Factor D (Consider therapy modification)

Dabrafenib

may lower the serum level of CYP2C9 substrates (High risk with Inducers). Treatment: Enzalutamide should not be used concurrently with CYP2C9 substrates that have a limited therapeutic index. Enzalutamide use, like with the use of any other CYP2C9 substrate, should be done with caution and under close observation.

Fosphenytoin

May lower the level of trimethoprim in the serum. Fosphenytoin's serum levels may rise when using trimethoprim. In order to prevent potentially decreased trimethoprim efficacy and higher phenytoin concentrations/effects, consider alternatives to this combination whenever it is practical. For each of these potential side effects, cautiously monitor patients receiving this combination.

Methotrexate

Methotrexate's harmful or toxic effects may be exacerbated by trimethoprim. Management: Take into account avoiding the simultaneous use of trimethoprim or sulfamethoxazole with methotrexate. Monitor for the emergence of methotrexate toxicity symptoms if administered concurrently (e.g., bone marrow suppression).

MiFEPRIStone

May elevate CYP2C9 substrates' serum levels (High risk with Inhibitors). Management: During and for two weeks after mifepristone treatment, use CYP2C9 substrates at the lowest dose advised and keep a close eye out for any negative effects.

Phenytoin

Trimethoprim may raise the level of phenytoin in the blood. Trimethoprim's serum levels may drop if you take phenytoin. In order to prevent potentially decreased trimethoprim efficacy and higher phenytoin concentrations/effects, consider alternatives to this combination whenever it is practical. For each of these potential side effects, cautiously monitor patients receiving this combination.

Procainamide

The active metabolite(s) of procainamide may be present at higher serum quantities when taking trimethoprim. Procainamide levels in the serum may rise when taking trimethoprim.

Sodium Picosulfate

Antibiotics may reduce Sodium Picosulfate's therapeutic impact. Management: If a patient previously used or is currently using an antibiotic, think about utilising an alternative product for bowel cleansing prior to a colonoscopy.

Typhoid Vaccine

The Typhoid Vaccine's therapeutic benefits may be reduced by antibiotics. The only strain impacted is the live attenuated Ty21a strain. Treatment: Patients receiving systemic antibacterial drugs should refrain from receiving the live attenuated typhoid vaccination (Ty21a). It is recommended to wait at least 3 days following the last dose of antibacterial medication before administering this vaccine.

Risk Factor X (Avoid combination)

Amodiaquine

The neutropenic impact of amodiaquine may be strengthened by trimethoprim.

BCG (Intravesical)

Amodiaquine's serum levels may rise in response to trimethoprim.

Cholera Vaccine

Antibiotics may lessen BCG's therapeutic effects (Intravesical).

Dofetilide

Trimethoprim may raise Dofetilide's serum levels.

Leucovorin Calcium-Levoleucovorin

May lessen Trimethoprim's therapeutic impact. When treating Pneumocystis jirovecii pneumonia, avoid taking leucovorin or levoleucovorin at the same time as trimethoprim (with sulfamethoxazole). Keep a close eye out for diminished efficacy if trimethoprim is being used for another reason.

Monitoring parameters:

Monitor CBC with differential counts, platelet count, liver function tests, bilirubin, serum potassium, serum creatinine, and BUN periodically in patients on long-term treatment.

How to administer Trimethoprim (Alprim)?

  • It is administered without regard to meals.
  • It may be administered with food or milk to reduce the gastrointestinal side effects. 

Mechanism of action of Trimethoprim (Alprim):

  • It inhibits bacterial nucleic acids synthesis and proteins by reversibly inhibiting dihydrofolate reductase. 
  • This causes the inhibition of folic acids conversion to tetrahydrofolate, which is active folate. It is necessary for the production of nucleic acids and proteins in bacteria.

Absorption:

  • When taken orally, it is easily absorbed.

Distribution:

  • It is found in many body tissues and fluids, including the middle ear, CSF, Bile and prostate.

Protein binding:

  • About 44%

Metabolism:

  • It undergoes demethylation, oxidation, and hydroxylation in the liver, where it is partially metabolised (10% to 20%).

Bioavailability:

  • Similar for tablets and solution

Half-life elimination:

  • Half-life elimination is prolonged with renal impairment
  • Newborns: 19 hours (range: 11 to 27 hours)
  • Infants 2 months to 1 year: 4.6 hours (range: 3 to 6 hours)
  • Children:
    • 1 to 3 years: 3.7 hours
    • 8 to 10 years: 5.4 hours
  • Adults with normal renal function: 8 to 10 hours

Time to peak serum concentration:

  • 1 to 4 hours

Excretion:

  • It is mainly eliminated in urine (between 50 and 60 percent of it as an unmodified medication);
  • feces

International Brand Names of Trimethoprim:

  • Primsol
  • Trimpex
  • Abaprim
  • Alprim
  • Antrin
  • Catin
  • Epirim
  • Giprim
  • Idotrim
  • Infectotrimet
  • Monotrim
  • Motrim
  • Primosept
  • Sinersul
  • Solotrim
  • Sulotrim
  • Tediprima
  • Tobyprim
  • Trimcort
  • Trimesan
  • Trimetin
  • Trimetop
  • Trimetoprim
  • Trimol-A
  • Trimopan
  • Trimoptin
  • Triprim
  • Urotrim
  • Utisept
  • Wellcoprim

Trimethoprim Brand Names in Pakistan:

Trimethoprim Suspension 80 mg in Pakistan

Zoprim-Ds Atlantic Pharmaceuticals (Pvt) Ltd.

 

Trimethoprim Suspension 40 mg/5ml in Pakistan

Royamax Semos Pharmaceuticals (Pvt) Ltd.
Zoprim Atlantic Pharmaceuticals (Pvt) Ltd.

 

Trimethoprim Tablets 160 mg in Pakistan

Incot-Ds Innvotek Pharmaceuticals

 

Trimethoprim Tablets 300 mg in Pakistan

Syraprim Glaxosmithkline