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CIPROFLOXACIN
(brand name: Cipro)
Pharmacological category:
antidyskinetic
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Reviews |
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| Cipro |
J Periodontol. 2004 Dec;75(12):1663-7.
Distribution of systemic ciprofloxacin and doxycycline
to gingiva and gingival crevicular fluid.
Lavda M, Clausnitzer CE, Walters JD.
Section of Periodontology, College of Dentistry, The Ohio State
University Health Sciences Center, Columbus, OH 43218-2357, USA.
BACKGROUND: Systemic fluoroquinolones and tetracyclines reach steady-state
levels in gingival crevicular fluid (GCF) that are several-fold higher
than their levels in serum. The mechanism by which this occurs is unclear,
but gingival fibroblasts are known to accumulate these agents. Uptake
by fibroblasts could enhance their distribution to gingiva. To test this
hypothesis, steady-state levels of these agents were assayed in serum,
gingival connective tissue (GCT), and GCF. METHODS: Healthy subjects who
needed resective periodontal surgery participated in the study. Approximately
78 hours prior to the surgical appointment, each subject began a 3-day
regimen of ciprofloxacin or doxycycline. At the surgical appointment (scheduled
approximately 6 hours after the last dose), samples of blood and GCT were
collected. GCF samples were collected on paper strips and measured with
an electronic device. Samples were extracted and analyzed by high performance
liquid chromatography. RESULTS: Mean ciprofloxacin levels in serum, GCT,
and GCF were 0.40 microg/ml, 1.38 microg/g, and 1.66 microg/ml, respectively
(P<0.001, N=9). For doxycycline, these levels were 1.11 microg/ml,
2.03 microg/g, and 2.41 microg/ml, respectively (P=0.002, N=8). For both
agents, the GCT and GCF levels were significantly higher than serum levels
(P<0.05), but not significantly different from each other. CONCLUSIONS:
Our findings suggest that fibroblasts could play an important role in
the distribution of fluoroquinolones and tetracyclines to the gingiva.
By accumulating these agents in GCT, fibroblasts could contribute to the
relatively high levels they attain in GCF.
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Ann Rheum Dis. 2003 Sep;62(9):880-4
Effect of a three month course of ciprofloxacin on the
late prognosis of reactive arthritis Yli-Kerttula
T, Luukkainen R, Yli-Kerttula U, Mottonen T, Hakola M, Korpela M, Sanila
M, Uksila J, Toivanen A
Department of Medicine, Turku University, Satalinna Hospital, Finland
BACKGROUND: The value of antibiotics in the treatment of reactive arthritis
(ReA) is still controversial. OBJECTIVES: To analyse the long term outcome
of patients with ReA, treated with a three month course of ciprofloxacin
or placebo. METHODS: Patients who had had ReA and had participated in a
double blind, placebo controlled trial on the effectiveness of ciprofloxacin
4-7 years earlier were invited to a clinical examination. Of the 71 patients
who were included in the original study, 53 agreed to visit the clinic for
an examination. Twenty six of 53 patients had originally received ciprofloxacin
and 27 had belonged to the placebo group. Of these, 20 in the ciprofloxacin
and 25 in the placebo group were HLA-B27 positive. RESULTS: 11/27 (41%)
patients in the original placebo group had now developed chronic rheumatic
disease, as compared with only 2/26 (8%) patients originally treated with
ciprofloxacin (p=0.006). Two patients who originally had received placebo,
none in the ciprofloxacin group had developed ankylosing spondylitis, and
three patients in the original placebo group, none in the ciprofloxacin
group had recurrent anterior uveitis. The same tendency was seen when several
different measures were analysed. Of the patients with chronic spondyloarthropathy,
10 in the placebo and none in the ciprofloxacin group were HLA-B27 positive.
CONCLUSION: Analysis 4-7 years after the initial ReA suggests that a three
month course of antibiotics in the acute phase may have a beneficial effect
on the long term prognosis. |
| Harefuah 2002 May;141
Spec No:63-72, 121, 120
Anthrax - an overview at 2002
Mozes YN, Winder A, Tadmor B, Rotman E, Sagi R, Hourvitz
A
Children's Ward A, Schneider Children's Medical Centre, Israel
BACKGROUND: Bacillus anthracis, the causative agent of anthrax, is well
known in human history as a major cause of disease in domestic and wild
animals and as a rare condition in humans. For the last seventy years,
anthrax was developed and occasionally stored as an agent of biological
weapon arsenal in numerous countries. The incubation period in humans
is 1-6 days and the disease may be present as three distinct clinical
syndromes: cutaneous, inhalational, and gastrointestinal disease. The
major concern in regard of biological warfare is the inhalational form
of anthrax, which starts as a febrile flu-like disease. The development
of malaise, fatigue, cough and mild chest discomfort is followed by severe
respiratory distress with dyspnea, diaphoresis, stridor, and cyanosis.
Shock and death occur within 24-36 hours after onset of severe symptoms.
Physical findings are non-specific, but a widened mediastinum is usually
seen on chest x-ray. A positive blood culture, immunohistochemical methods
and the use of the polymerase chain reaction method confirm the diagnosis.
Although effectiveness may be limited after severe symptoms are present,
a high dose of antibiotic treatment should be administered and aggressive
supportive therapy may be necessary. In the situation of an anthrax attack,
as was recently seen in the United States, penicillin is no longer recommended
as an acceptable first line therapy. In this case, ciprofloxacin or doxycycline
is the recommended drug of choice since penicillin-resistant strains may
be used, as well as the possibility of the emergence of an inducible beta-lactamase
positive bacterium. Since a high infecting dose may exacerbate the clinical
course of the disease, a combination antibiotic regimen should be considered.
The disease is not contagious and standard precautions are sufficient.
Pre-exposure prophylaxis is based on a vaccine administration, while post-exposure
prophylaxis is feasible by the initial use of oral ciprofloxacin or doxycycline.
In this article we reviewed the literature with emphasis on the recent
medical reports from the United States analyzing the eleven cases of inhalational
anthrax as well as the new guidelines for diagnosis and treatment that
resulted from the bioterrorism attack in October 2001. Although physical
findings were non-specific, abnormal findings on chest x-rays were present
in all the eleven cases. A positive blood culture, immunohistochemical
methods and the use of the polymerase chain reaction method were highly
valuable in revealing and confirming the diagnosis of anthrax. In the
case of an attack with anthrax spores, the likelihood of exposure to a
large infective dose of high quality spores, may require a prolonged period
of treatment as well as prolonged post-exposure therapy. |
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Drug information |
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| GENERIC NAME: ciprofloxacin
BRAND NAME: Cipro, Cipro XR
DRUG CLASS AND MECHANISM: Many common infections in humans
are caused by single cell organisms, called bacteria. Bacteria can grow
and multiply, infecting different parts of the body. Medicines that control
and eradicate these bacteria are called antibiotics. Ciprofloxacin is
an antibiotic that stops multiplication of bacteria by inhibiting the
reproduction and repair of their genetic material (DNA).
PREPARATIONS: Tablets: 250mg, 500mg, 750mg. Tablets
Cipro XR: 500 and 1000 mg.
STORAGE: Ciprofloxacin should be stored at below 86
degrees F.
PRESCRIBED FOR: Ciprofloxacin is used to treat infections
of the skin, lungs, airways, bones, and joints caused by susceptible bacteria.
Ciprofloxacin is also frequently used to treat urinary infections caused
by bacteria such as E. coli. Ciprofloxacin is effective in treating infectious
diarrheas caused by E. coli, campylobacter jejuni, and shigella bacteria.
DOSING: Ciprofloxacin may be taken with or without food.
Ciprofloxacin is partially metabolized by the liver and excreted by the
kidney. Dosages require adjustment in patients with severely abnormal
liver or kidney function. Antacids block the absorption of ciprofloxacin
and they should not be taken together.
DRUG INTERACTIONS: Ciprofloxacin administered together
with theophylline can lead to elevated blood levels of theophylline. Theophylline
is used to open airways in the treatment of asthma. Toxic levels of theophylline
can lead to seizures, and disturbances in heart rhythm. If concurrent
use of ciprofloxacin and theophylline cannot be avoided, frequent blood
tests to monitor theophylline blood levels are performed. Ciprofloxacin
should be used with caution in patients with central nervous system diseases
such as seizures, because rare seizures have been reported in patients
receiving this medication. Ciprofloxacin should be avoided in children
and adolescents under 18 years old, as safe use in these patients have
not been established.
Many antibiotics, including ciprofloxacin, can alter the normal bacteria
in the colon and encourage overgrowth of a bacteria responsible for the
development of inflammation of the colon (pseudomembranous colitis). Pseudomembranous
colitis can cause fever, abdominal pain, diarrhea, and sometimes even
shock. Patients taking ciprofloxacin can develop sensitivity of the skin
to direct sunlight. Ciprofloxacin can enhance the action of the anticoagulant
warfarin (Coumadin), and increase the risk of bleeding.
PREGNANCY: Ciprofloxacin should be avoided in pregnancy,
as safe use in these patients have not been established.
NURSING MOTHERS: Ciprofloxacin should be avoided in
nursing mothers, as safe use in these patients have not been established.
SIDE EFFECTS: The most frequent side effects include
nausea, vomiting, diarrhea, abdominal pain, rash, headache, and restlessness.
Rare allergic reactions have been described, such as hives and anaphylaxis
(shock).
Caution! Before starting
to take this medicine, it is vital that you should consult your doctor!
Do not use it on your own initiative, without medical advice.
Also, you should read carefully important health information about this
drug given here:
my.webmd.com |
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Order now ! |
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CIPRO (Ciprofloxacin)
Substance: Ciprofloxacin
Brand Name: Ciprobay
Manufacturer: Bayer Corporation
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Dosage |
Packing |
Price |
Pay now |
250 mg |
10 tab |
USD 21.00 |
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500 mg |
10 tab |
USD 43.00 |
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250 mg |
30 tab |
USD 57.00 |
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500 mg |
30 tab |
USD 119.00 |
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CIPRO - GENERIC
Substance: Ciprofloxacin
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Dosage |
Packing |
Price |
Pay now |
250 mg |
100 tab |
USD 43.00 |
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500 mg |
100 tab |
USD 59.00 |
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