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Bactrim liquid dose by using the volume, weight, and weight to volume method. A dose unit of Bactrim® containing 1 gram or 0.04 mg of penicillin could be given in the amount of 1 mL solution or the container containing liquid. One-half mL of Bactrim® could also be given intravenously in divided doses. After one-half mL of the solution is injected into an extremity, the extremity should be kept in an ice-covered, warm environment for one hour following the injection. Alternatively, solution could be given by the subcutaneous route. For this method, the intravenous route prescription drug prices us vs canada can be used. In some embodiments, the invention provides a pharmaceutical composition in dosage form for administration to a subject comprising Bactrim® including and an antimicrobial agent. The invention also provides a method of treating subject by administering an amount of a pharmaceutical composition comprised in Bactrim®-containing composition, the pharmaceutical composition comprising Bactrim® and the antimicrobial agent to one or more animals, the animals treated being selected from having the same clinical presentation as a particular human patient and/or animals having the same clinical presentation in a particular population such as geographical area or demographic grouping. An animal is a living or dead animal from which a pharmacologic effect has been produced when administered to a subject and/or of the study. Examples of dosage forms Bactrim® include, but are not limited to, the following: tablets and/or capsules, subcutaneous suppositories, ointments, emulsions and foams, drops, sprays, powders, each of such dosage forms can be used for any combination of these or otherwise depending upon the desired effect or indications. Examples of types appropriate for use, and use in combination, include, but are not limited to, tablets, capsules (in tablet or capsule-like formulations), tablets, capsules-like suspensions, powder preparations, capsules containing or other suitable containers, granule preparations, suspension foam suspension-like suspensions, ointments, creams, and elixirs suitable for topical use. In addition to the pharmaceutical composition as described above, Bactrim® may also be administered topically. Bactrim® can formulated as an ointment, which can then be applied to the exposed surface of a skin lesion or site of contact as a cream or oil which may then be dispensed into the affected area. In addition to the pharmaceutical composition, Bactrim® may also be administered by injection or transdermal administration. In addition to the pharmaceutical composition, a sterile, inert, preservative-free, or inert pharmaceutical carrier such as gelatin or lactose monohydrate a sterile, inert diluent such as polyethylene glycol, may be used to increase the stability of Bactrim®. However, any amount Bactrim® may be administered if desired. For purposes of this invention, the term "drug" is intended to include any substance, preferably a pharmaceutical composition and comprising drug, as well any other compound or mixture comprising a drug compound or mixture of two more drugs. The term "drug" is intended to exclude the compounds, such as natural or synthetic compounds which may be derived from a drug but the compounds may be non-toxic or have properties which may produce undesirable effects if combined in an unsupervised clinical setting. For example, the natural compounds or synthetic included herein are not intended to have therapeutic, toxic, or other non-pharmacologic effects. In general, the term "drug" is considered synonymous with "pharmaceutically acceptable salt" or "pharmaceutical composition." As used herein, the term "intranasal" also refers to oral or parenteral administration of any amount Bactrim® to a subject. As used herein, the term "analogical" refers to a compound whose pharmacological effects are related to those of another compound wherein the different compounds have differential stereoisomeric forms. For example an analog of penicillin with the N-termini exposed two carbons is an analog of penicillin but the derivative with two nitrogen atoms (P-N-T-C-C) is not an analog of penicillin if the N-terminus is exposed with one carbon. Additionally, analogs do not necessarily have identical pharmacological effects when in the same structure because pharmacokinetic parameters, such as the peak concentration and Cmax and/or time to maximum concentration (Tmax) can vary depending on the particular compound. As used herein, the term "antibiotic" means penicillin or derivatives of such that have antiviral activity against the following organisms: Bacilli, Streptococci, Mycobacteria,.

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