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Cephalexin is well absorbed orally with an absolute bioavailability of 75%. Cephalexin has a volume of distribution of approximately 2.7 L/kg and is only 20% bound to plasma proteins.
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Cephalexin may not work as well and may require higher doses to obtain the same effect as when originally taken.
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clinical trial was performed to assess the analgesic efficacy and reported side effects of Cephalexin 100 mg, Cephalexin 50 mg,
risk of discontinuation due to adverse events associated with higher initial doses,
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Intramuscular (i.m.) Cephalexin increases gastric pH during anaesthesia similar to famotidine.
Cephalexin 100 mg was statistically superior to placebo for TOTPAR, SPID, and time of remedication,
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Do not stop using this medication suddenly without first talking to your doctor.
Nonetheless, Cephalexin nearly doubled the interthreshold range at a concentration near 200 ng/mL.
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Check the label on the medicine for exact dosing instructions.Cephalexin may cause drowsiness and dizziness.
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The volume of distribution of Cephalexin was 2.6 and 2.9 liters/kg in male and female subjects, respectively,
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Check the label on the medicine for exact dosing instructions.Cephalexin may cause drowsiness and dizziness.
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Use Cephalexin with caution in the ELDERLY; they may be more sensitive to its effects.Cephalexin should not be used in CHILDREN younger than 16 years old;
which may affect the therapeutic response (see PRECAUTIONS - Drug Interactions).
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Check with your health care provider before you start, stop, or change the dose of any medicine.Use Cephalexin as directed by your doctor.
Cephalexin is well absorbed orally with an absolute bioavailability of 75%. Cephalexin has a volume of distribution of approximately 2.7 L/kg and is only 20% bound to plasma proteins.
The mean absolute bioavailability of a 100 mg oral dose is approximately 75%. The mean peak plasma concentration of racemic Cephalexin and M1 occurs at two and three hours, respectively, after administration in healthy adults.
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Cephalexin has been shown to inhibit reuptake of norepinephrine and serotonin in vitro,
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Cephalexin is well absorbed orally with an absolute bioavailability of 75%. Cephalexin has a volume of distribution of approximately 2.7 L/kg and is only 20% bound to plasma proteins.
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Forty patients were treated with either Cephalexin suppositories 100 mg 6 hourly (qds) or acetaminophen/codeine suppositories 1000/20 mg qds.
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Nalbuphine consumption in the first 24 h after operation was reduced by 35% in the Cephalexin group.
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Cephalexin may induce psychic and physical dependence of the morphine-type (?- opioid) (See WARNINGS).
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