The macrolides, lincosamides, and tetracyclines are primarily ___________ (inhibit bacterial growth) drugs and may be __________ (kill bacteria), depending on the drug dose or _________ (microorganism capable of producing disease).
bacteriostatic, bactericidal, pathogen
Glycopeptides, aminoglycosides, and fluoroquinolones are __________ drugs.
bactericidal
Drugs from these groups are used as penicillin substitutes, especially in individuals who are allergic to penicillin.
___________ is the drug frequently prescribed if the patient has a hypersensitivity to penicillin.
Erythromycin
Macrolides, including azithromycin (Zithromax), clarithromycin (Biaxin), and erythromycin (E-Mycin), are called __________________.
broad-spectrum antibiotics
the first macrolide
Erythromycin
__________ bind to the 50S ribosomal subunits and inhibit protein synthesis.
Macrolides
Gastric acid destroys erythromycin in the stomach; therefore, acid-resistant salts are added to erythromycin (e.g., ethylsuccinate, stearate, estolate) to decrease dissolution (breakdown in small particles) in the stomach. True or False?
True
___________ is the drug of choice for the treatment of mycoplasmal pneumonia and Legionnaire’s disease.
Erythromycin
_________ is clarithromycin in a once-a-day extended-release tablet to be taken for 7 days.
Biaxin XL
_____________ is frequently prescribed for upper and lower respiratory infections, STIs, and uncomplicated skin infections.
Azithromycin
Macrolides are excreted in bile, feces, and urine. Because only a small amount is excreted in urine, renal insufficiency is not a contraindication for macrolide use. True or False?
True
Side effects and adverse reactions to macrolides
GI disturbances such as nausea, vomiting, diarrhea, and abdominal cramping
_____________ may develop as a side effect of azithromycin.
Conjunctivitis
____________ can occur when erythromycin and azithromycin are taken in high doses with other hepatotoxic drugs, such as acetaminophen (high doses), phenothiazines, and sulfonamides.
Hepatotoxicity (liver toxicity)
Erythromycin should not be taken with clindamycin or lincomycin because
they compete for receptor sites. True or False?
True
To avoid severe toxic effects, erythromycin should not be used with other macrolides. True or False?
True
Macrolides can increase serum levels of these drugs
theophylline (bronchodilator)
carbamazepine (anticonvulsant)
warfarin (anticoagulant)
The first extended macrolide group developed after the introduction of erythromycin was _____________, which has been effective against many bacterial infections.
clarithromycin (Biaxin)
Elimination of extended macrolide group is via ___________.
bile and feces
Common side effects of clarithromycin and azithromycin
nausea, diarrhea, abdominal discomfort
Monitor patient for liver damage resulting from prolonged use and high dosage of macrolides such as azithromycin. Signs of liver dysfunction include elevated liver enzyme levels and jaundice. True or False?
True
In taking macrolides, teach patient to report any evidence of _____________ (a secondary infection resulting from
drug therapy), such as stomatitis or vaginitis.
superinfection
In taking macrolides, tell patient to report onset of loose stools or diarrhea. ____________________ should be ruled out.
Pseudomembranous colitis
examples of lincosamides
Clindamycin (Cleocin)
Lincomycin (Lincocin)
Which among the two is more widely prescribed than the other because it is active against most gram-positive organisms, including Staphylococcus aureus and anaerobic organisms? It is not effective against gram-negative bacteria (e.g., Escherichia coli, Proteus, Pseudomonas). Clindamycin or lincomycin?
Clindamycin
Side effects and adverse reactions to clindamycin and lincomycin
GI irritation, which may manifest as nausea, vomiting, and stomatitis, rash
Severe adverse reactions to clindamycin and lincomycin
colitis, anaphylactic shock
Clindamycin and lincomycin are incompatible with aminophylline, phenytoin (Dilantin), barbiturates, and ampicillin. True or False?
True
_______________, a glycopeptide bactericidal antibiotic, is used against drug-resistant S. aureus and in cardiac surgical prophylaxis for individuals with penicillin allergies. S
Vancomycin (Vancocin)
Vancomycin has become ineffective for treating ____________.
enterococci
______________________ is a combined antibacterial used to treat life-threatening vancomycin-resistant enterococci (VREF) infections.
Quinupristin/dalfopristin
_________________, a glycopeptide, treats selected gram-positive bacteria and skin infections. This drug is a semisynthetic derivative of vancomycin, with bactericidal action against MRSA.
Telavancin (Vibativ)
Vancomycin may cause ______________ and ____________.
nephrotoxicity, ototoxicity
______________ results in damage to the auditory or vestibular branch of cranial nerve VIII. Such damage can result in permanent hearing loss (auditory branch) or temporary or permanent loss of balance (vestibular branch).
Ototoxicity
Side effects of vancomycin
chills, dizziness, fever, rashes, nausea, vomiting, and thrombophlebitis at the injection site
Too rapid an IV injection of vancomycin can cause a condition known as
_____________________. Characterized by red blotching of the face, neck, and chest, this is a toxic effect rather than an allergic reaction.
“red man” syndrome or red neck syndrome
_______________ can mask ototoxicity when taken with vancomycin.
Dimenhydrinate (Dramamine)
The first drug in Ketolides is _______________, which is used for adults 18 years of age and older to treat mild to moderate community-acquired pneumonia.
telithromycin (Ketek)
Side effects and adverse reactions to telithromycin
visual disturbances (blurred vision and diplopia), headache, dizziness, altered taste, nausea, vomiting, diarrhea, and liver failure
Telithromycin may also lead to an exacerbation of ________________.
myasthenia gravis
_______________, isolated from Streptomyces aureofaciens in 1948, were the first broad-spectrum antibiotics effective against gram-positive and gram-negative bacteria and many other organisms—mycobacteria, rickettsiae, spirochetes, and chlamydiae, to name a few.
Tetracyclines
Tetracyclines are not effective against S. aureus (except for the newer tetracyclines), Pseudomonas, or Proteus. They can be used against _____________.
Mycoplasma pneumoniae
Tetracycline in combination with metronidazole and bismuth subsalicylate
is useful in treating ______________, a bacterium in the stomach that can cause a peptic ulcer.
Helicobacter pylori
For years, oral and topical tetracycline has been used to treat severe _____________. Low doses are usually prescribed to minimize the toxic effect of the drug.
acne vulgaris
Tetracycline resistance has increased in the treatment of pneumococcal and gonococcal infections; therefore tetracyclines are not as useful in treating these infections. True or False?
True
Because IM administration of tetracycline causes pain on injection and tissue irritation, this route of administration is seldom used. The _______ route is used to treat severe infections.
IV
______________ (sunburn reaction) may occur in persons taking tetracyclines, especially demeclocycline (Declomycin).
Photosensitivity
(Tetracycline) _______________ can cause damage to the vestibular part of the inner ear, which may result in difficulty maintaining balance.
Minocycline (Minocin)
______________ results when tetracycline is given in high doses with other nephrotoxic drugs.
Nephrotoxicity (kidney toxicity)
Because tetracycline can disrupt the microbial flora of the body, _________________ (secondary infection resulting from drug therapy) is another adverse reaction that might result.
superinfection
prevent absorption of tetracycline from the GI tract
Antacids (Maalox and others)
iron-containing drugs
inhibit tetracycline absorption
milk
drugs high in calcium
Lipid-soluble tetracyclines (doxycycline and minocycline) are actually
better absorbed from the GI tract when taken with milk products and food. True or False?
True
_____________ is an antibiotic in a category called glycylcycline, a synthetic analogue of the tetracyclines. This drug acts by blocking protein synthesis in bacterial cells, resulting in a bacteriostatic action.
Tigecycline (Tygacil)
Advise patient to check expiration date on bottle of tetracycline; out-of-date tetracycline can be toxic. True or False?
True
Female patients who are contemplating pregnancy can still take tetracycline because it has no teratogenic effect. True or False?
False. Inform female patients who are contemplating pregnancy to avoid taking tetracycline because of possible teratogenic effect.
Oral contraceptives may be less effective when given concurrently with tigecycline. Warfarin levels may be increased and may lead to bleeding when taken with tigecycline. True or False?
True
________________, derived from the bacterium Streptomyces griseus in 1944, was the first aminoglycoside available for clinical use and was used to treat tuberculosis. Because of its ototoxicity and the bacterial resistance that can develop, it is infrequently used today.
Streptomycin sulfate
Despite its toxicity, streptomycin is the drug of choice to treat __________ and __________________.
tularemia, bubonic pneumonic forms of plague
_____________ are for serious infections. These cannot be absorbed from the GI tract and cannot cross into the cerebrospinal fluid.
Aminoglycosides
IV aminoglycosides can be given with penicillins and cephalosporins but should not be mixed together in the same container.When combinations of antibiotics are given IV, the IV line is flushed after each antibiotic has been administered to ensure that the antibiotic was completely delivered. True or False?
True
Serious adverse reactions to aminoglycosides
ototoxicity and nephrotoxicity
In taking aminoglycosides, check for __________________. Aminoglycosides can cause ototoxicity.
hearing loss
The mechanism of action of _____________ is to interfere with the enzyme DNA gyrase, which is needed to synthesize bacterial deoxyribonucleic acid (DNA). Their antibacterial spectrum includes bactericidal action on both gram-positive and gram-negative organisms.
fluoroquinolones
the earliest derivatives of the fluoroquinolone group, prescribed primarily for urinary tract infection caused by common gram-negative organisms such as E. coli
Nalidixic acid (NegGram) and
cinoxacin (Cinobac)
This group of antibiotics is useful in the treatment of urinary tract, bone, and joint infections; bronchitis; pneumonia; gastroenteritis; and gonorrhea.
Fluoroquinolones
synthetic antibacterials related to nalidixic acid
Ciprofloxacin (Cipro) and norfloxacin (Noroxin)
(Fluoroquinolone) _______________ is used primarily to treat respiratory problems, such as community-acquired pneumonia, chronic bronchitis, acute sinusitis, urinary tract infections, and uncomplicated skin infections.
Levofloxacin (Levaquin)
(Fluoroquinolone) _____________ is available for once-a-day oral and parenteral dosing. This drug is prescribed to treat the same infections other fluoroquinolones are effective against.
Moxifloxacin is more active than levofloxacin against S. pneumoniae. True or False?
True
____________ is an FDA-approved antibiotic in the category of lipopeptides. It acts by binding to the bacterial membrane and causing rapid depolarization of its membrane potential, inhibiting protein, DNA, and RNA synthesis. This action results in bacterial cell death.
Daptomycin (Cubicin)
_________________ was discovered in 1947 and has a bacteriostatic action by inhibiting bacterial protein synthesis. Because of the toxic effects of chloramphenicol, including blood dyscrasias related to bone
marrow suppression, it is used only to treat serious infections.
Chloramphenicol (Chloromycetin)
Author
raine
ID
363536
Card Set
Macrolides, Tetracyclines, Aminoglycosides, and Fluoroquinolones