Clindamycin is a lincosamide antibiotic that works by binding to the 50S subunit of the bacterial ribosome, inhibiting protein synthesis. It has bacteriostatic or bactericidal effects depending on the susceptible bacteria. Common adverse effects include gastrointestinal issues like diarrhea and nausea, as well as genitourinary issues like vaginitis. Clindamycin should be administered with caution and monitoring of renal, hepatic, and hematologic functions during long-term use.
DESIGN, DEVELOPMENT AND IN-VITRO EVALUATION OF METOPROLOL TARTRATE FAST DISSOLVING TABLETS K. Ramesh Reddy, V. Jayasankar Reddy, G. Saisri Harsha, K.Anil
Clindamycin is a lincosamide antibiotic that works by binding to the 50S subunit of the bacterial ribosome, inhibiting protein synthesis. It has bacteriostatic or bactericidal effects depending on the susceptible bacteria. Common adverse effects include gastrointestinal issues like diarrhea and nausea, as well as genitourinary issues like vaginitis. Clindamycin should be administered with caution and monitoring of renal, hepatic, and hematologic functions during long-term use.
Clindamycin is a lincosamide antibiotic that works by binding to the 50S subunit of the bacterial ribosome, inhibiting protein synthesis. It has bacteriostatic or bactericidal effects depending on the susceptible bacteria. Common adverse effects include gastrointestinal issues like diarrhea and nausea, as well as genitourinary issues like vaginitis. Clindamycin should be administered with caution and monitoring of renal, hepatic, and hematologic functions during long-term use.
Clindamycin is a lincosamide antibiotic that works by binding to the 50S subunit of the bacterial ribosome, inhibiting protein synthesis. It has bacteriostatic or bactericidal effects depending on the susceptible bacteria. Common adverse effects include gastrointestinal issues like diarrhea and nausea, as well as genitourinary issues like vaginitis. Clindamycin should be administered with caution and monitoring of renal, hepatic, and hematologic functions during long-term use.
Generic/ Classification Mechanism of Action Consideration/ What to Adverse Effect
Brand Observe/ Look
Pharmacologic Antibacterial action: Drug • Take culture and sensitivity GI: esophagitis, nausea, vomiting, classification: lincomyci inhibits bacterial protein tests before treatment starts; abdominal pain, diarrhea, Clindamycin n derivative synthesis by binding to repeat as needed. pseudomembranous colitis. ribosome’s 50S subunit. • Don’t refrigerate Dosage: 200 Therapeutic Clindamycin may produce reconstituted oral solution GU: cervicitis, vaginitis, Candida mg. / BID classification: antibiotic bacteriostatic or because it will thicken. Drug albicans overgrowth, vulvar bactericidal effects on remains stable for 2 weeks at irritation. Pregnancy risk category susceptible bacteria, room temperature. B including most aerobic • I.M. preparation should be Hematologic: transient gram-positive cocci and given deep I.M. Rotate sites. leukopenia, eosinophilia, anaerobic gram-negative Doses exceeding 600 mg thrombocytopenia. and gram-positive aren’t recommended. organisms. It’s • I.M. injection may increase Hepatic: jaundice. considered a first-line creatine kinase levels drug in the treatment because of muscle irritation. Skin: maculopapular rash, of Bacteroides fragilis and • For I.V. infusion, dilute each urticaria, most other gram-positive 300 mg in 50 ml of D5W, dryness, redness, pruritus, and gram-negative normal saline solution, or swelling, irritation, contact anaerobes. It’s also lactated Ringer’s solution and dermatitis, burning. effective give no more than 30 against Mycoplasma mg/minute. Don’t administer Other: anaphylaxis. pneumoniae, Leptotrichia more than 1.2 g/hour. buccalis, and some gram- • Topical form may produce positive cocci and bacilli. adverse systemic effects. • Monitor renal, hepatic, and hematopoietic functions during prolonged therapy.
DESIGN, DEVELOPMENT AND IN-VITRO EVALUATION OF METOPROLOL TARTRATE FAST DISSOLVING TABLETS K. Ramesh Reddy, V. Jayasankar Reddy, G. Saisri Harsha, K.Anil