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Information about Ciprofloxacin (Cipro)*
Ciprofloxacin is the generic international name for the
synthetic antibiotic manufactured and sold by Bayer Pharmaceutical under the
brand name CiproŽ (and other brand names in other markets, e.g. veterinary
drugs), belonging to a group called fluoroquinolones. Ciprofloxacin is
bactericidal and its mode of action depends on blocking of bacterial DNA
replication by binding itself to an enzyme called DNA gyrase, which allows the
untwisting required to replicate one DNA double helix into two. Notably the drug
has 100 times higher affinity for bacterial DNA gyrase than for mammalian.
Activity
Ciprofloxacin is a broad-spectrum antibiotic that is active against both
Gram-positive and Gram-negative bacteria.
Enterobacteriaceae
Vibrio
Hemophilus influenzae
Neisseria gonorrhoeae
Neisseria menigitidis
Moraxella catarrhalis
Brucella
Campylobacter
Mycobacterium intracellulare
Legionella sp.
Pseudomonas aeruginosa
Bacillus anthracis - that causes anthrax
Weak activity against:
Streptococcus pneumoniae
No activity against:
Bacteroides
Burkholderia cepacia
Enterococcus faecium
Ureaplasma urealyticum
and others
The major adverse effect seen with use of is gastrointestinal irritation, common
with many antibiotics. Because of its general safety, potency and broad spectrum
activity, ciprofloxacin was initially reserved as a 'last-resort' drug for use
on difficult and drug-resistant infections. As with any antibiotic, however,
increasing time and usage has led to an increase in ciprofloxacin-resistant
infections, mainly in the hospital setting. Also implicated in the rise of
resistant bacteria is the use of lower-cost, less potent fluoroquinolones, and
the widespread addition of ciprofloxacin and other antibiotics to the feed of
farm animals, which leads to greater and more rapid weight gain, for reasons
which are not clear.
Label information
The drug is available for oral and parenteral use. It is used in lower
respiratory infections (pneumonias), urinary tract infections, STDs,
septicemias, Legionellosis and atypical Mycobacterioses. Dosage in respiratory
infections is 500-1500 mg a day in 2 doses.
It is contraindicated in children, pregnancy, and in patients with epilepsy.
Dose adjustment or avoidance may be necessary with liver or renal failure.
Ciprofloxacin can cause photosensitivity reactions and can elevate plasma
theophylline levels to toxic values. It can also cause constipation and
sensitivity to caffeine.
Interactions
Quercetin, a flavonoid occasionally used as a dietary supplement may interact
with fluroquinolones, as quercetin competitively binds to bacterial DNA gyrase.
Some foods such as garlic and apples contain high levels of quercetin. Whether
this inhibits or enhances the effect of Fluoroquinolones is not immediately
clear (Hilliard et al 2004).
Contraindications
Metal cations such as aluminum, magnesium, calcium, ferrous sulfate, and zinc
are thought to form chelation complexes with fluoroquinolone antibiotics and
prevent the drugs from being absorbed. Because of this, avoid taking antacids
which contain aluminum, magnesium or calcium with ciprofloxacin. Sucralfate,
which has a high aluminum content, also reduces the bioavailability of
ciprofloxacin to approximately 4% (Spivey et al 1996). Ciprofloxacin may be
taken with meals or on an empty stomach. Ciprofloxacin should NOT be taken with
dairy products or calcium-fortified juices alone, but may be taken with a meal
that contains these products. [1]
Heavy exercise is discouraged, as achilles tendon rupture has been reported in
patients taking ciprofloxacin.
The toxicity of drugs that are metabolised by the cytochrome P450 system is
enhanced by concomitant use of some quinolones. They may also interact with the
GABA A receptor and cause neurological symptoms; this is further augmented by
certain non-steroidal anti-inflammatory drugs (Brouwers 1992).
Business aspects
The discovery and development of ciprofloxacin is that rare case of an actual
groundbreaking new drug development, opening up an entire new class of
antibiotics for further research, development, and marketing. Even more
remarkable, it seems to be a case where the first drug discovered of this class
remains the 'gold standard' in terms of efficacy, with the other drugs developed
by other pharmaceutical companies relegated to 'me-too' status and forced to
compete on the basis of lower cost.
Encouraged by the magnitude of this success, as well as the influx of cash,
Bayer Pharmaceutical embarked on a plan to remake itself from a minor
pharmaceutical manufacturer into a major player in the international
pharmaceutical business, with a lock on the antibiotic field. Unfortunately, a
combination of the tendency for antibiotics to be viewed as a commodity and
prescribed on the basis of lowest cost, Bayer's inability to follow up with
another 'blockbuster' discovery, and a general downturn in the international
pharmaceutical business forced Bayer into a major downsizing in 2000-2001. Faced
with the imminent expiration of its patent rights to ciprofloxacin in the early
2000's and the predictable loss of market share to generic ciprofloxacin, Bayer
has resorted to the usual strategy of pharmaceutical companies in such a
situaton; focus on the development and patenting of new variations of the old
drug (i.e. pediatric ciprofloxacin, intravenous ciprofloxacin, once-a-day
ciprofloxacin, etc.), which will have the side effect of extending the patent on
the original drug.
"Cipro" became a household word during the anthrax mail attacks after the
destruction of the World Trade Center. Unfortunately, Bayer not only took a
severe financial blow from the costs involved in rapidly increasing production
of the drug to be sold to the government at far below market price, but
ironically was then portrayed in the press as 'War Profiteers', rather than
contributors to the safety of the public in the "War on Terror".
The source of this article is
Wikipedia, the free encyclopedia. The text of this
article is licensed under the
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