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Muhammad Asad Sardar
Group Brand Manager
WHAT IS UNIVERSALLY ACCLAIMED?
UNICLIN-Introduction:
• Broad-spectrum
• Semi-synthetic Antibiotic
• Bactericidal Antibiotic
• Clindamycin is in a same class of
medications called Lincosamides.
• It works by slowing or stopping the
growth of bacteria.
MODE OF ACTION:
• Lincosamides prevent bacteria
replicating by interfering with the
synthesis of proteins.
• They bind to the 23s portion of the 50S
subunit of bacterial ribosomes and cause
premature dissociation from the
ribosome.
DO LINCOSAMIDES REACT WITH
HUMAN CELLS?
• Lincosamides do not interfere with
protein synthesis in human cells (or those
of other eukaryotes) because human
ribosomes are structurally different from
those of bacteria.
SIDE EFFECTS:
More common• Abdominal or stomach cramps and pain
• Abdominal tenderness
• Diarrhea (watery and severe), which may also be bloody
• Fever
Less common• Sore throat and fever
• Skin rash, redness, and itching
• Unusual bleeding
IN PREGNANCY:
• Clindamycin has been assigned to pregnancy category B by the FDA (Animal reproduction studies have failed to demonstrate a risk to the fetus and there are no adequate and well-controlled studies in pregnant women.)
• Clindamycin has been used during pregnancy and labor and delivery without adverse effects in the fetus or neonate.
• Clindamycin is only recommended for use during pregnancy when benefit outweighs risk.
IN NURSING MOTHER:
• A Concentrations of 0.7 to 3.8 mcg/mL of Clindamycin have been reported into human milk.
• Adverse gastrointestinal effects have been reported in one nursing infant exposed to multiple drugs including Clindamycin.
• Due to the potential for adverse effects in neonates, a decision should be made to discontinue nursing or discontinue the drug.
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• The penicillins have historically been used
as the first-line therapy in Odontogenic
Infections, but increasing rates of resistance
have lowered their usefulness.
• Clindamycin is an attractive first-line
therapy in the treatment of Odontogenic
infections.
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FEATURES & BENEFITS:
• Excellent Penetration
• Lower MICs
• Safe & Tolerable
• Quality with Economy
• Simple & Convenient Dosage
PSEUDOMEMBRANOUS COLITIS
• Pseudomembranous colitis is infection of the large intestine (colon) with an overgrowth of Clostridium difficile bacteria***.
• The Clostridium difficile bacteria is normally seen in the intestine. However, it may overgrow when you take antibiotics. The bacteria release a powerful toxin that causes the lining of the colon to become inflamed and bleed***.
• The most common antibiotics associated with this condition are ampicillin, clindamycin, fluoroquinolones, and cephalosporin***.
Incidence:• Incidence rates for clindamycin-induced
pseudomembranous colitis are reported as 0.1% to 10%*
• The results suggest that the risks associated with the use of Clindamycin are acceptable if the drug is given for the approved specific indications.**
• Pseudomembranous colitis is rare in infants younger than 12 months old and uncommon in children***.
**Med J Aust. 1977 Feb 19;1(8):243-6
Take medication before half an hour of meal with full glass of
water.
References:
*Infectious Diseases in Children, January 2005
**Med J Aust. 1977 Feb 19;1(8):243-6
***Cohen SH, Gerding DN, Johnson S, et al. Clinical practice guidelines for Clostridium difficile infection in adults: 2010 update by the Society for Healthcare Epidemiology of America (SHEA) and the Infectious Diseases Society of America (IDSA). Infect Control Hosp Epidemiol. 2010;31(5):431-455.
***Gerding DN, Johnson S. Clostridial infections. In: Goldman L, Schafer AI, eds. Cecil Medicine. 24th ed. Philadelphia, Pa: Saunders Elsevier; 2011:chap 304.
***Thielman NM, Wilson KH. Antibiotic-associated colitis. In: Mandell GL, Bennett JE, Dolin R, eds. Principles and Practice of Infectious Diseases. 7th ed. Philadelphia, Pa: Elsevier Churchill Livingstone; 2009:chap 96.
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