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Trimethoprim 50 mg tablet and at 4 weeks, or 3 months and at 8 months. In patients with ALM, treatment trimethoprim 50 mg tablet is not needed during all three clinical periods or at the beginning of three clinical periods. Therefore, trimethoprim 50 mg tablet may be withheld in the patient with an established infection of the skin or eye; and in the patients without such an immune deficiency as a result of chemotherapy or immune suppressants. Precautions The following contraindications to trimethoprim 50 mg tablet should be noted: (i) Any patient taking trimethoprim 100 mg tablets (without an oral contraceptive) with any other medication. When combining the trimethoprim 50 mg tablets with other medications the effect of trimethoprim should not be decreased. (ii) Acute diarrhea due to hepatitis C. difficile infection (C. diff). (iii) Any patient suffering from ulcerative colitis. (iv) Prolonged duration of antibiotics. (v) Patients on hemodialysis. (vi) Hypersensitivity to the active ingredient. Contraindications The contraindications listed in Table 1 apply to treatment with the trimethoprim 50 mg tablet and its formulations. Use in Patients with Known Hypersensitivity to TMG, PTP, TP or LTP Due to the potential for hypersensitivity reactions in patients with known hypersensitivity to TMG, TP, LTP or a combination thereof, trimethoprim 50 mg tablets should NOT be used in patients with known allergies to TMG, TP, LTP or a combination thereof. These patients should be closely monitored after initiating treatment for symptoms of hypersensitivity to this compound or combination thereof TMG, LTP a thereof. The risk for allergy associated with use of trimethoprim 50 mg tablet in these patients is expected to be substantially lower than that encountered with use other agents of the class. When symptoms hypersensitivity occur (see PRECAUTIONS: General: Acute Inpatient Care: Illness). When prescribing trimethoprim 50 mg tablet or when it is desired to reduce the use of this product, trimethoprim 50 mg tablet should be prescribed sparingly in patients whom other anticoagulant agents have been or may be necessary. The safety and effectiveness of trimethoprim 50 mg tablet have not been established in children. If used children, trimethoprim 50 mg tablet should be administered with caution and should NOT be divided or added to the other triclosan containing products. Drug Identification Number trimethoprim 50 mg tablet, USP Rx Only Drug Name Sulfoxaflor NDC Number 598947000 Medically reviewed on September 5, 2018 This medicine has not been identified by the FDA as being misbranded or otherwise unfit for other uses according to the law. Disclaimer: The information contained on this site is provided for informational purposes only. The information does not take into consideration the medical needs, special allergies or other considerations of any specific patient. You should always consult with your doctor or pharmacist regarding medicines and medical decisions. Copyright 2018 Truven Health Analytics, LLC.
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