Introduction

Ciprobay and ciprofloxacin are both fluoroquinolone antibiotics, and their main pharmacologic target are the bacterial infections. The ciprofloxacin class of antibiotics has been widely studied since the 1940s and has an active spectrum of activity, and the quinolone class of antibiotics have been used to treat a wide range of infections. The efficacy of ciprofloxacin against a wide range of bacterial infections has been demonstrated in numerous clinical trials and, to a limited extent, in animal models and humans. However, the use of ciprofloxacin has been limited by the side effect profile of the drug. Furthermore, ciprofloxacin has been associated with a risk of developing anthrax, which is currently considered a public health emergency. In addition, there are a number of adverse events that can occur when using ciprofloxacin, and the adverse events reported to the FDA have been associated with ciprofloxacin use.

Ciprofloxacin is an antibiotic of the fluoroquinolone class that has been extensively studied and approved for the treatment of bacterial infections in humans and animals. The risk of developing anthrax when using ciprofloxacin has been reported to be 0.3-1% in animals and humans, and approximately 2% in humans, but it has been reported that there are no reports of anthrax in pregnant women, and the risk of exposure to anthrax is rare [].

In addition to the potential risk of exposure to anthrax, there are some reports of exposure to anthrax in animals []. The most common adverse events reported to the FDA and to the FDA-approved drug safety program, however, are gastrointestinal, hepatotoxicity, and photosensitivity. These adverse events were reported to the FDA in association with ciprofloxacin use. In contrast, the most common adverse events reported to the FDA-approved drug safety program, including the photosensitivity, were not associated with ciprofloxacin use. The incidence of the common adverse events reported to the FDA-approved drug safety program was 4.8% in pregnant animals and 2.6% in animal models. These reports have been published in peer-reviewed journals and the FDA has not approved these reports. The most common adverse events reported to the FDA-approved drug safety program in pregnant animals were gastrointestinal symptoms [, ]. The most common adverse events reported to the FDA-approved drug safety program, including the photosensitivity, were not associated with ciprofloxacin use. The most common adverse events reported to the FDA-approved drug safety program in animal models were not associated with ciprofloxacin use. The adverse events reported to the FDA-approved drug safety program in pregnant animals were not associated with ciprofloxacin use.

In addition, there are a number of adverse events that can occur when using ciprofloxacin, and these adverse events were not associated with ciprofloxacin use. These adverse events were reported to the FDA-approved drug safety program in animals and humans. However, the incidence of the common adverse events reported to the FDA-approved drug safety program in pregnant animals was not associated with ciprofloxacin use. The incidence of the common adverse events reported to the FDA-approved drug safety program in animal models was 4.8% in pregnant animals and 2.6% in animal models, but the risk of exposure to anthrax is rare [].

Materials and Methods

Human Subjects

All human subjects who met the inclusion criteria were recruited from the Department of Veterinary Medicine of the Faculty of Medicine of University of Luec-Aplenas (Spain) from July 2013 to July 2014. The study was approved by the Institutional Review Board (IRB) of the Faculty of Medicine of the University of Luec-Aplenas (approval number: LSEI_0014) and the Ethics Committee of the Hospital Universitario Universitario de Luec-Aplenas (approval number: HUA_0219). All subjects provided written informed consent prior to the study. The subjects were included in the study if they had an adequate knowledge of human medicine and had an adequate knowledge of the use of ciprofloxacin in the treatment of bacterial infections.

Indications

Treatment of bacterial infections of the lungs, nose, ear, bones and joints, skin and soft tissue, kidney, bladder, abdomen, and genitals caused by ciprofloxacin-susceptible organisms. Infections may include urinary tract infection, prostatitis, lower respiratory tract infection, otitis media (middle ear infection), sinusitis, skin, bone and joint infections, infectious diarrhea, typhoid fever, and gonorrhea.

Administration

May be taken with or without food. May be taken w/ meals to minimise GI discomfort. Do not take w/ antacids, Fe or dairy products.

Contraindication

Hypersensitivity to ciprofloxacin or other quinolones. History or risk of QT prolongation; known history of myasthenia gravis. Concomitant use with tizanidine.

Common side-effects

Vomiting, Stomach pain, Nausea, Diarrhea

Special Precaution

Patient with known or suspected CNS disorders, risk factors predisposing to seizures, or lower seizure threshold; history or risk factors for QT interval prolongation, torsades de pointes, uncorrected hypokalaemia/hypomagnesaemia, cardiac disease (e.g. heart failure, MI, bradycardia); positive family history of aneurysm disease, pre-existing aortic aneurysm or dissection and its risk factors (e.g. Marfan syndrome, vascular Ehlers-Danlos syndrome, hypertension, peripheral atherosclerotic vascular disease); diabetes, previous tendon disorder (e.g. rheumatoid arthritis), G6PD deficiency. Renal and hepatic impairment. Elderly, children. Pregnancy and lactation.

Storage

Store between 20-25°C.

MedsGo Class

Quinolones

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MedsGo Interaction

General

MedsGo Mechanism of Action

Toxins reduce efficacy of an antiprotozoal therapy by antagonizing bacterial DNA gyrase and topoisomerase IV. Toxins may also inhibit efficacy of bacterial products. Toxins may increase levels of cyclic guanosine monophosphate (cGMP), resulting in increased heart rate, oligoclonal bands, myoclonal bands, and myoclonus. Toxins may increase levels of nitric oxide, resulting in increased heart rate, increased blood pressure, increased blood urea and increased liver enzyme levels. Toxins may alter levels of cyclic guanosine monophosphate (cGMP), resulting in increased heart rate, increased oligoclonal bands, myoclonal bands, and myoclonus. Toxins may enhance effects of bacterial products, including levels of cGMP. cGMP may reduce efficacy of an antiprotozoal therapy by affecting DNA topoisomerase IV. Toxins may also increase levels of cyclic guanosine monophosphate (cGMP), resulting in increased heart rate, increased oligoclonal bands, myoclonus, and myoclonus. cGMP levels may decrease with use of antibiotics. Toxins may enhance effects of bacterial products, such as levels of cGMP. cGMP may increase with use of antibiotics. Bacterial products may antagonise bacterial DNA gyrase and topoisomerase IV.

Adults

Infections may include urinary tract infection, prostatitis, lower respiratory tract infection, urethral and sinusitis, infectious diarrhea, typhoid fever, and gonorrhea. The above includes other uses as well.

Ciprofloxacin: Antibiotic

Ciprofloxacin is a drug that belongs to a group of medicines called fluoroquinolones. It is used to treat certain bacterial infections. It works by stopping the growth of certain bacteria. Ciprofloxacin works by blocking the enzymes that break down DNA. Ciprofloxacin is used to treat a variety of bacterial infections.

How do you take ciprofloxacin?

It is best to take Ciprofloxacin as your doctor has prescribed. You should take it at the same time every day. You should take the medicine with a full glass of water. You should avoid consuming this medicine unless your doctor has told you otherwise. Ciprofloxacin will work best in a small dose. Your doctor may adjust the dose or make other recommendations. It is best to take your medicine at the same time each day. You should take Ciprofloxacin at the same time every day. If you miss a dose, do not take it unless it is time to take it. Do not take a double dose to make up for a missed one.

What are the side effects of Ciprofloxacin?

Ciprofloxacin can cause side effects in some people. These side effects may include:

Some of the side effects of Ciprofloxacin include:

Some of the side effects of Ciprofloxacin may not affect everyone. If you experience any of the side effects, talk to your doctor. Your doctor can help you if you have any side effects.

Drug interactions with Ciprofloxacin

Some drugs interact with Ciprofloxacin. This is because some medicines and foods can affect the way Ciprofloxacin works.

Tell your doctor if you have any drug interactions. They may include:

Cuprofloxacin tablets and Ciprofloxacin capsules may reduce the effectiveness of the medicine and make it less effective. It may also cause the blood sugar to fall. This will make your blood sugar less effective.

Do not share Ciprofloxacin with others, even if they have the same condition as you. If you take Ciprofloxacin and a companion of yours, it may not work as well. You should tell your doctor before taking Ciprofloxacin, even if you are in the same family as them. They may want to check your blood sugar level while you are taking Ciprofloxacin.

What should I tell my doctor before taking Ciprofloxacin?

Tell your doctor if you have ever had an allergic reaction to ciprofloxacin or any other medicine.

Tell your doctor if you are pregnant or breastfeeding. Ciprofloxacin can pass into the breast milk. Your doctor will want to monitor your baby for any possible side effects. Your doctor may want to change your dose or prescribe a different medicine. They may recommend a different medicine to treat your infection.

Are there any interactions with ciprofloxacin?

There may be interactions between Ciprofloxacin and other medicines, such as blood thinners. This is because some medicines and foods can interact with Ciprofloxacin.

Tell your doctor if you have kidney problems, low blood pressure, or other health problems. They may want to check your blood pressure while you are taking ciprofloxacin.

Tell your doctor if you have any liver problems, stomach or bowel problems, or kidney disease. You should tell your doctor if you are pregnant or breastfeeding. Ciprofloxacin passes into breast milk. Your doctor will want to check your baby for any possible side effects.

Tell your doctor if you are allergic to Ciprofloxacin or any other medicines, foods, or other substances. This may cause some of the side effects.

If you are pregnant or breast-feeding, tell your doctor.

Ciprofloxacin 500mg/1ml Suspension 40ml

₹40Original price was: ₹40.Current price is: ₹40.

Ciprofloxacin 500mg/1ml Suspension 40ml is a fluoroquinolone antibiotic used to treat a wide range of bacterial infections, including respiratory tract infections, urinary tract infections, skin and soft tissue infections, and certain sexually transmitted infections like gonorrhea. Ciprofloxacin 500mg/1ml Suspension 40ml prevents the growth and multiplication of bacteria in the body. It will not kill the infection. This medication is not recommended for use by pregnant or breastfeeding women.

Note:The actual product packaging may vary slightly from the images shown on our website. Due to manufacturer updates, there may be variations in packaging design. We strive to provide accurate representations of all products.

Uses:

• treats a range of bacterial infections: pneumonia, ear, nose, and throat infections, bronchitis, and sinus infections.
• preventes the spread of sexually transmitted infections like gonorrhea and syphilis.

Dosage:

• 400 mg taken orally twice a day for 7 days.
• 500 mg taken orally once a day for 7 days.
• 600 mg taken orally once a day for 7 days.
• 800 mg taken orally once a day for 7 days.

Therapeutic Category:

• Ciprofloxacin
• Other quinolone antibiotics.

Delivery:

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• All other drugs are restricted to medical supervision.

Side Effects:

• Allergic reactions like rash, itching, swelling, severe dizziness, trouble breathing, chest pain, confusion, trouble sleeping, nausea, vomiting, and stomach pain.

Precautions:

• Take Ciprofloxacin with food and other liquid. Avoid taking in larger or smaller quantities or for longer than recommended. Drug interactions may change the results of the medication. Consult your doctor or pharmacist for more details.
• Inform your doctor if you have liver or kidney problems. Ciprofloxacin may affect the results of blood tests. Your doctor will decide the best treatment option based on the results. Remember that your doctor has prescribed Ciprofloxacin because you have used the medication correctly.
• Ciprofloxacin may cause dizziness or fainting.