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Acyclovir (Therapeutic Classification)
Viral DNA Polymerase Inhibitor TherapeuticClassification
Acyclovir (FDA Label Indication)
Genital Herpes (active and suppressive), Herpes zoster, Varicella (chickenpox), cold sores FDALabelIndication
Acyclovir (Pregnancy Category)
None PregnancyCategory
Acyclovir (Box Warning)
None BoxWarning
Acyclovir (Common Adverse Drug Reaction)
Headaches, Elevated LFTs CommonAdverseDrugReaction
Acyclovir (Mechanism of Action)
Acyclovir is an acyclic nucleoside analogue of deoxyguanosine that is selectively phosphorylated by the virus-encoded thymidine kinase to its monophosphate form. Cellular enzymes then convert the monophosphate to the active antiviral acyclovir triphosphate, which competitively inhibits viral DNA synthesis by inactivation of viral DNA polymerase and incorporation into and termination of viral DNA replication. Acyclovir has potent activity against HSV I and II and HZV (VZV). MechanismofAction
Acyclovir (Key Patient Counseling Points)
Complete full course of therapy; administer with high-fat meals or grapefruit juice. Avoid pregnancy for at least 1 mo posttreatment. In children or those with difficulty swallowing tablets, tablets can be crushed or chewed and swallowed with water. Patients with nematode infection should wash underwear and bedding often in hot water to prevent recurrent infections KeyPatientCounselingPoints
Acyclovir (Brand Name)
Zovirax BrandName
Zovirax (Generic Name)
Acyclovir BrandToGeneric
Amoxicillin (Therapeutic Classification)
β-Lactam Antibiotic TherapeuticClassification
Amoxicillin (FDA Label Indication)
Acute otitis media; lower respiratory tract infection; Strep pharyngitis; ear,nose and throat infection; infection of skin and genitourinary system; H. pylori FDALabelIndication
Amoxicillin (Pregnancy Category)
None PregnancyCategory
Amoxicillin (Box Warning)
None BoxWarning
Amoxicillin (Common Adverse Drug Reaction)
Diarrhea, nausea CommonAdverseDrugReaction
Amoxicillin (Mechanism of Action)
Semisynthetic penicillin derivative that inhibits the biosynthesis of bacterial cell wall mucopeptide. Typically active against Streptococcus, Enterococcus, Staphylococcus, and Enterobacteriaceae. MechanismofAction
Amoxicillin (Key Patient Counseling Points)
Complete full course of therapy. For the suspension, shake well and store in the refrigerator. Note short expiration after reconstitution. Can take with food if causes upset stomach. Avoid mixing suspension with food or beverages and use with measuring device that comes with prescription. Symptoms should improve within 2-3 d; if they worsen, seek follow-up with health-care practitioner. May decrease effectiveness of oral contraceptives; encourage patients to use backup contraceptive method (eg, condom) KeyPatientCounselingPoints
Amoxicillin (Brand Name)
Amoxil, Moxatag, Trimox BrandName
Amoxil, Moxatag, Trimox (Generic Name)
Amoxicillin BrandToGeneric
Amoxicillin; Clavulanate Potassium (Therapeutic Classification)
β-Lactam Antibiotic TherapeuticClassification
Amoxicillin; Clavulanate Potassium (FDA Label Indication)
Acute otits media;CAP; lower respiratory infection; Sinusitis, infection of skin, genitourinary system; UTI acute cystitis, UTI pyelonephritis FDALabelIndication
Amoxicillin; Clavulanate Potassium (Pregnancy Category)
None PregnancyCategory
Amoxicillin; Clavulanate Potassium (Box Warning)
None BoxWarning
Amoxicillin; Clavulanate Potassium (Common Adverse Drug Reaction)
Nausea, diarrhea CommonAdverseDrugReaction
Amoxicillin; Clavulanate Potassium (Mechanism of Action)
Amoxicillin is a semisynthetic penicillin derivative. Typically active against Streptococcus, Enterococcus, Staphylococcus, and Enterobacteriaceae. Amoxicillin is not effective against β-lactamase-producing bacteria. Clavulanate, a β-lactamase inhibitor, has weak antibacterial activity but is a potent inhibitor of plasmid-mediated β-lactamases and protects amoxicillin from degradation by β-lactamases. MechanismofAction
Amoxicillin; Clavulanate Potassium (Key Patient Counseling Points)
Complete full course of therapy. Take dose with food to ensure proper absorption. For the suspension, shake well and store in the refrigerator. Note short expiration after reconstitution of 10 d. Avoid mixing suspension with food or beverages. Symptoms should improve within 2-3 d; if they worsen, seek follow-up with health-care practitioner. May decrease effectiveness of oral contraceptives; encourage patients to use backup contraceptive method (eg, condom). KeyPatientCounselingPoints
Amoxicillin; Clavulanate Potassium (Brand Name)
Augmentin (XR) BrandName
Augmentin (XR) (Generic Name)
Amoxicillin; Clavulanate Potassium BrandToGeneric
Azithromycin (Therapeutic Classification)
Macrolide TherapeuticClassification
Azithromycin (FDA Label Indication)
Acute infective exacerbation of COPD, skin/tissue infection; Bacterial sinusitis, Chancroid, nongonococcal cervicitis, nongonococcal urethritis; CAP; STIs; Strep pharyngitis FDALabelIndication
Azithromycin (Pregnancy Category)
None PregnancyCategory
Azithromycin (Box Warning)
None BoxWarning
Azithromycin (Common Adverse Drug Reaction)
Diarrhea, nausea, vomiting CommonAdverseDrugReaction
Azithromycin (Mechanism of Action)
Azithromycin is a macrolide antibiotic that is slightly less active than erythromycin against gram-positive bacteria but substantially more active against M. (B.), Haemophilus sp., Legionella sp., Neisseria sp., Bordetella sp., Mycoplasma sp., and C. trachomatis. Azithromycin binds to the 50S ribosomal subunit, thus interfering with microbial protein synthesis. MechanismofAction
Azithromycin (Key Patient Counseling Points)
Complete full course of therapy. Take tablets with or without food, although some patients report increased tolerability when given with food. Avoid mixing suspension with food or beverages, but food can be taken afterward. Symptoms should improve within 2-3 d; if they worsen, seek follow-up with health-care practitioner. KeyPatientCounselingPoints
Azithromycin (Brand Name)
Zithromax BrandName
Zithromax (Generic Name)
Azithromycin BrandToGeneric
Cefdinir (Therapeutic Classification)
3rd-Gen Cephalosporin TherapeuticClassification
Cefdinir (FDA Label Indication)
Acute otits media, pharyngitis, tonsillitis; Bronchitis, acute & secondary; CAP; COPD acute exacerbation; Strep pharyngitis FDALabelIndication
Cefdinir (Pregnancy Category)
None PregnancyCategory
Cefdinir (Box Warning)
None BoxWarning
Cefdinir (Common Adverse Drug Reaction)
Diarrhea CommonAdverseDrugReaction
Cefdinir (Mechanism of Action)
Cefdinir is a 3rd-generation cephalosporin with activity against a number of gram-positive and gram-negative bacteria including β-lactamase-producing strains MechanismofAction
Cefdinir (Key Patient Counseling Points)
Complete full course of therapy. For the suspension, shake well and can be stored at room temperature. Note 10 d expiration after reconstitution. Avoid mixing suspension with food or beverages, but food can be taken afterward. Symptoms should improve within 2-3 d; if they worsen, seek follow-up with HCP. Separate administration of antacids, iron, and vitamins by 2 h. KeyPatientCounselingPoints
Cefdinir (Brand Name)
Omnicef BrandName
Omnicef (Generic Name)
Cefdinir BrandToGeneric
Cephalexin (Therapeutic Classification)
1st-Gen Cephalosporin TherapeuticClassification
Cephalexin (FDA Label Indication)
Infection of skin and/or subcutaneous tissue; Osteomyelitis; Otitis media; Strep pharyngitis; Impetigo, ethyma; Cellulitis, erysipelas FDALabelIndication
Cephalexin (Pregnancy Category)
None PregnancyCategory
Cephalexin (Box Warning)
None BoxWarning
Cephalexin (Common Adverse Drug Reaction)
Nausea CommonAdverseDrugReaction
Cephalexin (Mechanism of Action)
Cephalexin is a 1st-generation cephalosporin that inhibits bacterial wall synthesis of actively dividing cells by binding to ≥1 penicillin-binding proteins (PBPs). Most gram-positive bacteria, including non-penicillinase- and penicillinase-producing staphylococci and streptococci. Activity against gram-negative bacteria is less than that observed with the 2nd- and 3rd-generation cephalosporins and is primarily restricted to E. coli, Klebsiella, and Proteus mirabilis. MechanismofAction
Cephalexin (Key Patient Counseling Points)
Seek medical attention if rash develops. Complete full course of therapy. For the suspension, shake well and store in the refrigerator. Note short expiration after reconstitution. Avoid mixing suspension with food or beverages, but food can be taken afterward. Symptoms should improve within 2-3 d; if they worsen, seek follow-up with health-care practitioner. KeyPatientCounselingPoints
Cephalexin (Brand Name)
Keflex BrandName
Keflex (Generic Name)
Cephalexin BrandToGeneric
Ciprofloxacin (Therapeutic Classification)
Fluoroquinolone TherapeuticClassification
Ciprofloxacin (FDA Label Indication)
Anthrax; Bacterial prostatits, chronic; Bronchitis, lower respiratory tract infection, infection of bone, skin or soft tissue, abdomen, sinusitis; UTI FDALabelIndication
Ciprofloxacin (Pregnancy Category)
*Contraindicated PregnancyCategory
Ciprofloxacin (Box Warning)
Serious adverse effects (tendon rupture, peripheral neuropathy, CNS), exacerbation of myasthenia gravis BoxWarning
Ciprofloxacin (Common Adverse Drug Reaction)
Tooth discoloration in infants, musculoskeletal signs and symptoms CommonAdverseDrugReaction
Ciprofloxacin (Mechanism of Action)
Ciprofloxacin is a fluoroquinolone that inhibits bacterial DNA gyrase. It is highly active against aerobic, gram-negative bacilli. MechanismofAction
Ciprofloxacin (Key Patient Counseling Points)
Seek medical attention if decreased urination, yellowing of eyes, blistering skin rash or extreme fatigue, unusual bruising or bleeding, shortness of breath or chest pain, tendon pain, muscle weakness, a "pins and needles" tingling or pricking sensation, numbness in the arms or legs, confusion or hallucinations. Take with or without food, but not with milk or other dairy products. Take ciprofloxacin at least 2 h before or 6 h after antacids, sucralfate, or mineral supplements and multivitamins with calcium, iron, or zinc. If using the suspension, shake well before use; suspension may be stored at room temperature. KeyPatientCounselingPoints
Ciprofloxacin (Brand Name)
Cipro (XR) BrandName
Cipro (XR) (Generic Name)
Ciprofloxacin BrandToGeneric
Clindamycin (Therapeutic Classification)
Lincosamide Antibiotic TherapeuticClassification
Clindamycin (FDA Label Indication)
Bacterial infectious disease, susceptible infections due to anaerobic organisms, staph, strep, pneumococci; Injection of skin; Infectious disease of abdomen; lower respiratory tract infection; pelvic inflammatory disease; septicemia; osteomyelitis; diabetic foot infection FDALabelIndication
Clindamycin (Pregnancy Category)
None PregnancyCategory
Clindamycin (Box Warning)
Colitis BoxWarning
Clindamycin (Common Adverse Drug Reaction)
Nausea CommonAdverseDrugReaction
Clindamycin (Mechanism of Action)
Clindamycin is a semisynthetic 7-chloro-7-deoxylincomycin derivative that is active against most gram-positive organisms except enterococci and Clostridium. difficile. Gram-negative aerobes are resistant, but most anaerobes are sensitive. It inhibits bacterial protein synthesis by binding to the 50S ribosomal subunit; it is bactericidal or bacteriostatic depending on the concentration, organism, and inoculums. MechanismofAction
Clindamycin (Key Patient Counseling Points)
Complete full course of therapy. Symptoms should improve within 2-3 d; if they worsen, seek follow-up with HCP. Take with full glass of water. Remain upright for 30 min after dose to minimize risk of GI ulceration. KeyPatientCounselingPoints
Clindamycin (Brand Name)
Cleocin (oral, topical) BrandName
Cleocin (oral, topical) (Generic Name)
Clindamycin BrandToGeneric
Doxycycline (Therapeutic Classification)
Tetracycline Antibiotic TherapeuticClassification
Doxycycline (FDA Label Indication)
Acinetobacter infection; Acne vulgaris; Gonorrhea, uncomplicated; Staph infection; Pneumonia, CAP FDALabelIndication
Doxycycline (Pregnancy Category)
*Contraindicated 2nd & 3rd PregnancyCategory
Doxycycline (Box Warning)
None BoxWarning
Doxycycline (Common Adverse Drug Reaction)
Esophageal injury, photosensitivity; skin hyperpigmentation, tooth discoloration in children < 8 CommonAdverseDrugReaction
Doxycycline (Mechanism of Action)
Doxycycline is a broad-spectrum bacteriostatic compound that inhibits protein synthesis at the 30S ribosomal subunit. Activity includes gram-positive, gram-negative, aerobic, and anaerobic bacteria, as well as spirochetes, mycoplasmas, rickettsiae, chlamydiae, and some protozoa. Many bacteria have developed plasmid-mediated resistance. MechanismofAction
Doxycycline (Key Patient Counseling Points)
May take with food that does not contain calcium. Complete full course of therapy. Symptoms should improve within 2-3 d. May cause photosensitivity; discontinue at first sign of skin erythema. Wear sunscreen and avoid prolonged exposure to sunlight and ultraviolet light. Administer with 240 mL of water. KeyPatientCounselingPoints
Doxycycline (Brand Name)
Vibramycin, Doxy 100 BrandName
Vibramycin, Doxy 100 (Generic Name)
Doxycycline BrandToGeneric
Fluconazole (Therapeutic Classification)
Imidazole Antifungal TherapeuticClassification
Fluconazole (FDA Label Indication)
Candidal vulvovaginitis, uncomplicated & complicated; Candidiasis, systemic; Cryptococcal meningitis; Oropharyngeal candidiasis FDALabelIndication
Fluconazole (Pregnancy Category)
None PregnancyCategory
Fluconazole (Box Warning)
None BoxWarning
Fluconazole (Common Adverse Drug Reaction)
Headache CommonAdverseDrugReaction
Fluconazole (Mechanism of Action)
Fluconazole inhibits biosynthesis of ergosterol or other sterols, damaging the fungal cell wall membrane and altering its permeability MechanismofAction
Fluconazole (Key Patient Counseling Points)
Many medications, including OTC medications, interact with fluconazole. Do not take any new medications without consulting your doctor or pharmacist. If taking a weekly dose, take on same day and time each week KeyPatientCounselingPoints
Fluconazole (Brand Name)
Diflucan BrandName
Diflucan (Generic Name)
Fluconazole BrandToGeneric
Ketoconazole (Therapeutic Classification)
Imidazole Antifungal TherapeuticClassification
Ketoconazole (FDA Label Indication)
Candidiasis of skin; Dandruff; Pityriasis versicolor; Seborrheic dermatitis; Tinea corporis; Tinea cruris; Tinea pedis FDALabelIndication
Ketoconazole (Pregnancy Category)
None PregnancyCategory
Ketoconazole (Box Warning)
None BoxWarning
Ketoconazole (Common Adverse Drug Reaction)
Application site reaction with foam CommonAdverseDrugReaction
Ketoconazole (Mechanism of Action)
Ketoconazole inhibits biosynthesis of ergosterol or other sterols, damaging the fungal cell wall membrane and altering its permeability MechanismofAction
Ketoconazole (Key Patient Counseling Points)
Apply thin layer to affected area of skin. Skin should be intact. Do not get it in your eyes, nose, mouth, or vagina. Do not wash the areas where you applied this medicine for at least 3 h after application. Cosmetics (makeup or sunscreens) may be put on the affected areas 20 min after application. Topical products are alcohol based and flammable immediately after application. KeyPatientCounselingPoints
Ketoconazole (Brand Name)
Nizoral, Extina, Ketozole, Nizoral A-d, Xolegel (topical cream, gel, foam, shampoo) BrandName
Nizoral, Extina, Ketozole, Nizoral A-d, Xolegel (topical cream, gel, foam, shampoo) (Generic Name)
Ketoconazole BrandToGeneric
Levofloxacin (Therapeutic Classification)
Fluroquinolone Antibiotic TherapeuticClassification