Neofloxacin Uses

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What is Neofloxacin?

Neofloxacin injection is used to treat bacterial infections in many different parts of the body. It is also used to prevent an anthrax infection after a person has been exposed to anthrax. Neofloxacin is also used to treat and prevent plague (including pneumonic and septicemic plague).

Neofloxacin belongs to the class of medicines known as quinolone antibiotics. It works by killing bacteria or preventing their growth. However, Neofloxacin will not work for colds, flu, or other virus infections.

Neofloxacin is to be given only by or under the direct supervision of your doctor.

Neofloxacin indications

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To reduce the development of drug-resistant bacteria and maintain the effectiveness of Neofloxacin Tablets, USP and other antibacterial drugs, Neofloxacin Tablets, USP should be used only to treat or prevent infections that are proven or strongly suspected to be caused by susceptible bacteria. When culture and susceptibility information are available, they should be considered in selecting or modifying antibacterial therapy. In the absence of such data, local epidemiology and susceptibility patterns may contribute to the empiric selection of therapy.

Neofloxacin Tablets, USP is indicated for the treatment of adults (≥18 years of age) with mild, moderate, and severe infections caused by susceptible isolates of the designated microorganisms in the conditions listed in this section.

Culture and susceptibility testing

Appropriate culture and susceptibility tests should be performed before treatment in order to isolate and identify organisms causing the infection and to determine their susceptibility to Neofloxacin Tablets, USP. Therapy with Neofloxacin Tablets, USP may be initiated before results of these tests are known; once results become available, appropriate therapy should be selected.

As with other drugs in this class, some isolates of Pseudomonas aeruginosa may develop resistance fairly rapidly during treatment with Neofloxacin Tablets, USP. Culture and susceptibility testing performed periodically during therapy will provide information about the continued susceptibility of the pathogens to the antimicrobial agent and also the possible emergence of bacterial resistance.

Nosocomial Pneumonia

Neofloxacin Tablets, USP is indicated for the treatment of nosocomial pneumonia due to methicillin-susceptible Staphylococcus aureus, Pseudomonas aeruginosa, Serratia marcescens, Escherichia coli, Klebsiella pneumoniae, Haemophilus influenzae, or Streptococcus pneumoniae. Adjunctive therapy should be used as clinically indicated. Where Pseudomonas aeruginosa is a documented or presumptive pathogen, combination therapy with an anti-pseudomonal β-lactam is recommended.

Community-Acquired Pneumonia: 7–14 day Treatment Regimen

Neofloxacin Tablets, USP is indicated for the treatment of community-acquired pneumonia due to methicillin-susceptible Staphylococcus aureus, Streptococcus pneumoniae (including multi-drug-resistant Streptococcus pneumoniae [MDRSP]), Haemophilus influenzae, Haemophilus parainfluenzae, Klebsiella pneumoniae, Moraxella catarrhalis, Chlamydophila pneumoniae, Legionella pneumophila, or Mycoplasma pneumoniae.

MDRSP isolates are strains resistant to two or more of the following antibacterials: penicillin (MIC ≥2 mcg/mL), 2nd generation cephalosporins, e.g., cefuroxime, macrolides, tetracyclines and trimethoprim/sulfamethoxazole.

Community-Acquired Pneumonia: 5-day Treatment Regimen

Neofloxacin Tablets, USP is indicated for the treatment of community-acquired pneumonia due to Streptococcus pneumoniae (excluding multi-drug-resistant isolates [MDRSP]), Haemophilus influenzae, Haemophilus parainfluenzae, Mycoplasma pneumoniae, or Chlamydophila pneumoniae

Acute Bacterial Sinusitis: 5-day and 10–14 day Treatment Regimens

Neofloxacin Tablets, USP is indicated for the treatment of acute bacterial sinusitis due to Streptococcus pneumoniae, Haemophilus influenzae, or Moraxella catarrhalis.

Acute Bacterial Exacerbation of Chronic Bronchitis

Neofloxacin Tablets, USP is indicated for the treatment of acute bacterial exacerbation of chronic bronchitis due to methicillin-susceptible Staphylococcus aureus, Streptococcus pneumoniae, Haemophilus influenzae, Haemophilus parainfluenzae, or Moraxella catarrhalis.

Complicated Skin and Skin Structure Infections

Neofloxacin Tablets, USP is indicated for the treatment of complicated skin and skin structure infections due to methicillin-susceptible Staphylococcus aureus, Enterococcus faecalis, Streptococcus pyogenes, or Proteus mirabilis.

Uncomplicated Skin and Skin Structure Infections

Neofloxacin Tablets, USP is indicated for the treatment of uncomplicated skin and skin structure infections (mild to moderate) including abscesses, cellulitis, furuncles, impetigo, pyoderma, wound infections, due to methicillin-susceptible Staphylococcus aureus, or Streptococcus pyogenes.

Chronic Bacterial Prostatitis

Neofloxacin Tablets, USP is indicated for the treatment of chronic bacterial prostatitis due to Escherichia coli, Enterococcus faecalis, or methicillin-susceptible Staphylococcus epidermidis.

Complicated Urinary Tract Infections: 5-day Treatment Regimen

Neofloxacin Tablets, USP is indicated for the treatment of complicated urinary tract infections due to Escherichia coli, Klebsiella pneumoniae, or Proteus mirabilis.

Complicated Urinary Tract Infections: 10-day Treatment Regimen

Neofloxacin Tablets, USP is indicated for the treatment of complicated urinary tract infections (mild to moderate) due to Enterococcus faecalis, Enterobacter cloacae, Escherichia coli, Klebsiella pneumoniae, Proteus mirabilis, or Pseudomonas aeruginosa.

Acute Pyelonephritis: 5 or 10-day Treatment Regimen

Neofloxacin Tablets, USP is indicated for the treatment of acute pyelonephritis caused by Escherichia coli, including cases with concurrent bacteremia.

Uncomplicated Urinary Tract Infections

Neofloxacin Tablets, USP is indicated for the treatment of uncomplicated urinary tract infections (mild to moderate) due to Escherichia coli, Klebsiella pneumoniae, or Staphylococcus saprophyticus.

Inhalational Anthrax (Post-Exposure)

Neofloxacin Tablets, USP is indicated for inhalational anthrax (post-exposure) to reduce the incidence or progression of disease following exposure to aerosolized Bacillus anthracis. The effectiveness of Neofloxacin Tablets, USP is based on plasma concentrations achieved in humans, a surrogate endpoint reasonably likely to predict clinical benefit. Neofloxacin has not been tested in humans for the post-exposure prevention of inhalation anthrax. The safety of Neofloxacin in adults for durations of therapy beyond 28 days or in pediatric patients for durations of therapy beyond 14 days has not been studied. Prolonged Neofloxacin therapy should only be used when the benefit outweighs the risk.

Plague

Neofloxacin Tablets, USP is indicated for treatment of plague, including pneumonic and septicemic plague, due to Yersinia pestis (Y. pestis) and prophylaxis for plague in adults and pediatric patients, 6 months of age and older. Efficacy studies of Neofloxacin could not be conducted in humans with plague for ethical and feasibility reasons. Therefore, approval of this indication was based on an

efficacy study conducted in animals.

How should I use Neofloxacin?

Use Neofloxacin tablets as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Ask your health care provider any questions you may have about how to use Neofloxacin tablets.

Uses of Neofloxacin in details

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Use: Labeled Indications

Treatment of community-acquired pneumonia, including multidrug-resistant strains of Streptococcus pneumoniae (MDRSP); nosocomial pneumonia; chronic obstructive pulmonary disease, acute exacerbation; rhinosinusitis, acute bacterial (ABRS); prostatitis (chronic bacterial); urinary tract infection (uncomplicated or complicated); acute pyelonephritis; skin or skin structure infections (uncomplicated or complicated); inhalational anthrax (postexposure) to reduce incidence or disease progression; prophylaxis and treatment of plague (pneumonic and septicemic) due to Yersinia pestis

Limitations of use: Because fluoroquinolones have been associated with disabling and potentially irreversible serious adverse reactions (eg, tendinitis and tendon rupture, peripheral neuropathy, CNS effects), reserve Neofloxacin for use in patients who have no alternative treatment options for acute exacerbation of chronic bronchitis, acute bacterial sinusitis, and uncomplicated urinary tract infections.

Off Label Uses

Anthrax

Based on the Centers for Disease Control and Prevention (CDC) expert panel meetings on prevention and treatment of anthrax in adults, Neofloxacin is an effective and recommended agent for treatment of cutaneous anthrax and a recommended alternative agent for systemic anthrax.

Bite wound infection, prophylaxis or treatment (animal or human bite)

Based on the Infectious Diseases Society of America (IDSA) guidelines for the diagnosis and management of skin and soft tissue infections (SSTIs), Neofloxacin, in combination with metronidazole or clindamycin, is an effective and recommended alternative option for treatment of bite wounds, particularly in patients with a human bite wound who are hypersensitive to beta-lactams.

Cervicitis or urethritis due to Chlamydia trachomatis infection

Based on the CDC sexually transmitted diseases treatment guidelines, Neofloxacin is an effective and recommended alternative agent in the treatment of cervicitis or urethritis due to C. trachomatis infection.

Diabetic foot infection

Based on the IDSA guideline for diagnosis and treatment of diabetic foot infections, Neofloxacin, in combination with clindamycin, is an effective and recommended treatment option for diabetic foot infections.

Epididymitis, acute

Based on the CDC sexually transmitted diseases treatment guidelines, Neofloxacin is an effective and recommended agent in the treatment acute epididymitis most likely caused by sexually transmitted chlamydia, gonorrhea, and enteric organisms in men who practice insertive anal sex (in combination with ceftriaxone) or for acute epididymitis most likely caused by enteric organisms (as monotherapy).

Helicobacter pylori eradication

Based on the American College of Gastroenterology clinical guideline for the treatment of Helicobacter pylori infection, Neofloxacin is an effective and recommended component of a multiple-drug regimen for the treatment of H. pylori infection.

Intra-abdominal infection, complicated, community-acquired

Based on the Surgical Infection Society (SIS) and IDSA guidelines for the diagnosis and management of complicated intra-abdominal infections, Neofloxacin, in combination with metronidazole, is an effective and recommended treatment option for empiric therapy of complicated community-acquired intra-abdominal infections when resistance rates are less than 10% to 20%.

Neutropenia (chemotherapy-induced), antibacterial prophylaxis

Data from 2 randomized, double-blind, placebo-controlled trials support the use of oral Neofloxacin for prophylaxis of bacterial infections in patients receiving myelosuppressive chemotherapy ).

Travelers' diarrhea

Based on the CDC Yellow Book, the IDSA practice guidelines for the diagnosis and management of infectious diarrhea, and the American College of Gastroenterology guideline for the diagnosis, treatment, and prevention of acute diarrheal infections in adults, Neofloxacin is an effective and recommended treatment option for the management of travelers' diarrhea.

Tuberculosis

Based on the American Thoracic Society, CDC, and IDSA guidelines for the treatment of tuberculosis, Neofloxacin is an effective and recommended alternative agent for treatment of drug-resistant tuberculosis caused by sensitive organisms or when first-line agents are intolerable.

Neofloxacin description

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Each tablet contains Levofloxacin 250 mg as active ingredient corresponding to Neofloxacin hemihydrate 256.23 mg.

Neofloxacin also contains the following inactive ingredients: Sodium chloride; sodium hydroxide; hydrochloric acid (qs: pH 4.8) and water for injection for a volume of 100 mL (Na+ concentration: 154 mmol/L).

Neofloxacin is a synthetic broad-spectrum antibacterial agent for oral and IV administration. Chemically, Neofloxacin, a chiral fluorinated carboxyquinolone, is the pure (-)-(S)-enantiomer of the racemic drug substance ofloxacin. Neofloxacin is (-)-(S)-9-fluoro-2,3-dihydro-3-methyl-10-(4-methyl-1-piperazinyl)-7-oxo-7H-pyrido[1,2,3-de]-1,4 benzoxazine-6-carboxylic acid hemihydrate.

Its empirical formula is C18H20FN3O4·½H2O and its molecular weight is 370.38.

Neofloxacin is a light yellowish-white to yellow-white crystal or crystalline powder. The molecule exists as a zwitterion at the pH conditions in the small intestine. The data demonstrate that from pH 0.6-5.8, the solubility of Neofloxacin is essentially constant (approximately 100 mg/mL). Neofloxacin is considered soluble to freely soluble in this pH range, as defined by USP nomenclature. Above pH 5.8, the solubility increases rapidly to its maximum at pH 6.7 (272 mg/mL) and is considered freely soluble in this range. Above pH 6.7, the solubility decreases and reaches a minimum value (about 50 mg/mL) at a pH of approximately 6.9. Neofloxacin has the potential to form stable coordination compounds with many metal ions. This in vitro chelation potential has the following formation order: A1+3 > Cu+2 > Zn+2 > Mg+2 > Ca+2.

Neofloxacin dosage

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Dosage in Adult Patients with Normal Renal Function

The usual dose of Neofloxacin

Oral Solution is 250 mg, 500 mg, or 750 mg administered orally every 24 hours, as indicated by infection and described in Table 1.

These recommendations apply to patients with creatinine clearance ≥ 50 mL/min. For patients with creatinine clearance <50 mL/min, adjustments to the dosing regimen are required.

Dosage in Pediatric Patients

The dosage in pediatric patients ≥ 6 months of age is described below in Table 2.

Dosage Adjustment in Adults with Renal Impairment

Administer Neofloxacin with caution in the presence of renal insufficiency. Careful clinical observation and appropriate laboratory studies should be performed prior to and during therapy since elimination of Neofloxacin may be reduced.

No adjustment is necessary for patients with a creatinine clearance ≥ 50 mL/min.

In patients with impaired renal function (creatinine clearance <50 mL/min), adjustment of the dosage regimen is necessary to avoid the accumulation of Neofloxacin due to decreased clearance.

Table 3 shows how to adjust dose based on creatinine clearance.

Drug Interaction With Chelation Agents: Antacids, Sucralfate, Metal Cations, Multivitamins

Neofloxacin

Oral Solution

Neofloxacin

Oral Solution should be administered at least two hours before or two hours after antacids containing magnesium, aluminum, as well as sucralfate, metal cations such as iron, and multivitamin preparations with zinc or didanosine chewable/buffered tablets or the pediatric powder for oral solution.

Administration Instructions

Food and Neofloxacin

Oral Solution

It is recommended that Neofloxacin

Oral Solution be taken 1 hour before or 2 hours after eating.

Hydration for Patients Receiving Neofloxacin

Oral Solution

Adequate hydration of patients receiving oral Neofloxacin should be maintained to prevent the formation of highly concentrated urine. Crystalluria and cylindruria have been reported with quinolones.

Neofloxacin interactions

See also:
What other drugs will affect Neofloxacin?

To avoid incomplete absorption of oral Neofloxacin, antacids containing magnesium hydroxide and/or aluminium hydroxide should not be used concomitantly. The administration of these drugs are recommended at least 2 hrs before or 2 hrs after Neofloxacin administration.

The studies showed that there are no significant interactions between Neofloxacin with theophylline, warfarin, cyclosporin, digoxin, probenecid and cimetidine. However, concomitant administration of other quinolones with the drugs previously mentioned may change the pharmacokinetic and pharmacodynamic properties significantly. Therefore, the drugs listed as follows must be considered if Neofloxacin is co-administered:

Theophylline: Theophylline levels should be closely monitored and appropriate dosage adjustments made.

Warfarin: Prothrombin time or other suitable anticoagulation test should be monitored.

Cyclosporin: No significant clinical changes, hence no dosage adjustment of cyclosporin or Neofloxacin is required.

Digoxin: No significant clinical changes, hence no dosage adjustment of digoxin or Neofloxacin is required.

The concomitant administration of NSAID with a quinolone, including Neofloxacin, may increase the risk of CNS stimulation and convulsive seizures.

Disturbances of blood glucose, including hyperglycemia and hypoglycemia, have been reported in patients receiving quinolones concomitantly with oral antidiabetic drugs. Therefore, careful monitoring of blood glucose is recommended when these agents are co-administered.

Neofloxacin side effects

See also:
What are the possible side effects of Neofloxacin?

Serious and Otherwise Important Adverse Reactions

The following serious and otherwise important adverse drug reactions are discussed in greater detail in other sections of labeling:

Hypotension has been associated with rapid or bolus intravenous infusion of Neofloxacin. Neofloxacin should be infused slowly over 60 to 90 minutes, depending on dosage.

Crystalluria and cylindruria have been reported with quinolones, including Neofloxacin. Therefore, adequate hydration of patients receiving Neofloxacin should be maintained to prevent the formation of a highly concentrated urine.

Clinical Trial Experience

Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice.

The data described below reflect exposure to Neofloxacin in 7537 patients in 29 pooled Phase 3 clinical trials. The population studied had a mean age of 50 years (approximately 74% of the population was < 65 years of age), 50% were male, 71% were Caucasian, 19% were Black. Patients were treated with Neofloxacin for a wide variety of infectious diseases. Patients received Neofloxacin doses of 750 mg once daily, 250 mg once daily, or 500 mg once or twice daily. Treatment duration was usually 3 to 14 days, and the mean number of days on therapy was 10 days.

The overall incidence, type and distribution of adverse reactions was similar in patients receiving Neofloxacin doses of 750 mg once daily, 250 mg once daily, and 500 mg once or twice daily. Discontinuation of Neofloxacin due to adverse drug reactions occurred in 4.3% of patients overall, 3.8% of patients treated with the 250 mg and 500 mg doses and 5.4% of patients treated with the 750 mg dose. The most common adverse drug reactions leading to discontinuation with the 250 and 500 mg doses were gastrointestinal (1.4%), primarily nausea (0.6%); vomiting (0.4%); dizziness (0.3%); and headache (0.2%). The most common adverse drug reactions leading to discontinuation with the 750 mg dose were gastrointestinal (1.2%), primarily nausea (0.6%), vomiting (0.5%); dizziness (0.3%); and headache (0.3%).

Adverse reactions occurring in ≥1% of Neofloxacin-treated patients and less common adverse reactions, occurring in 0.1 to <1% of Neofloxacin-treated patients, are shown in Table 6 and Table 7, respectively. The most common adverse drug reactions (≥3%) are nausea, headache, diarrhea, insomnia, constipation, and dizziness.

In clinical trials using multiple-dose therapy, ophthalmologic abnormalities, including cataracts and multiple punctate lenticular opacities, have been noted in patients undergoing treatment with quinolones, including Neofloxacin. The relationship of the drugs to these events is not presently established.

Postmarketing Experience

Table 8 lists adverse reactions that have been identified during post-approval use of Neofloxacin. Because these reactions are reported voluntarily from a population of uncertain size, reliably estimating their frequency or establishing a causal relationship to drug exposure is not always possible.

Neofloxacin contraindications

See also:
What is the most important information I should know about Neofloxacin?

Patients hypersensitive to Neofloxacin or any other quinolones or any excipients of Neofloxacin. Patients with epilepsy and those with history of tendon disorder related to fluoroquinolone administration.

Use in pregnancy: Neofloxacin caused no impairment of fertility or reproductive performance in rats at oral doses as high as 360 mg/kg/day. It was not teratogenic in rats at oral doses as high as 810 mg/kg/day or at IV dose up to 160 mg/kg/day. No teratogenicity was observed when rabbits were dosed orally as high as 50 mg/kg/day.

In the absence of human data and due to the experimental risk of damage by fluoroquinolones to the weight-bearing cartilage of the growing organism, Neofloxacin must not be used in pregnant women or women suspected of being pregnant.

Use in lactation: In the absence of human data and due to the experimental risk of damage by fluoroquinolones to the weight-bearing cartilage of the growing organism, Neofloxacin must not be used in breastfeeding women.

Use in children: Safety and effectiveness in pediatric patients and adolescents <16 years have not been established. Quinolones, including Neofloxacin, cause arthropathy and osteochondrosis in juvenile animals of several species.

Use in

Elderly: The pharmacokinetic properties of Neofloxacin in younger adults and elderly do not differ significantly when creatinine clearance is taken into consideration. However, since Neofloxacin is known to be substantially excreted by the kidney, the risk of toxic reactions to Neofloxacin may be greater in patients with impaired renal function. Because elderly patients are more likely to have decreased renal function, care should be taken in dose selection and it may be useful to monitor renal function.



Active ingredient matches for Neofloxacin:

Levofloxacin in Bulgaria.


List of Neofloxacin substitutes (brand and generic names)

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Unit description / dosage (Manufacturer)Price, USD
Nblox 500mg TAB / 100 (N.B. Healthcare)$ 8.86
Neofus 100 mg x 10 Blister x 10 Tablet
Newgene Nevoraxin 100 mg x 1 Blister x 10 Tablet
Nirliv 500mg INF / 100ml (Nirma (Nirlife))$ 1.14
NIRLIV 500MG TABLET 1 strip / 10 tablets each (Nirma (Nirlife))$ 0.02
NIRLIV INFUSION 1 bottle / 100 ML infusion each (Nirma (Nirlife))$ 0.33
NIRLIV infusion 500 mg x 100ml (Nirma (Nirlife))$ 1.14
Nirliv inj 500 mg/100 mL / / plastic 1's (Nirma (Nirlife))
Nirliv 500mg Tablet (Nirma (Nirlife))$ 0.00
Nirliv NA Infusion (Nirma (Nirlife))$ 0.00
Nislev 500 mg x 1 x 10's (Pharos)$ 35.90
Nislev IV 500 mg/100 mL x 1's (Pharos)$ 20.46
Nokicef 200 mg Tablet (Foregen Healthcare Pvt. Ltd.)$ 0.18
NOKICEF 200 MG TABLET 1 strip / 10 tablets each (Foregen Healthcare Pvt. Ltd.)$ 1.33
Nokicef 200mg Tablet (Foregen Healthcare Pvt. Ltd.)$ 0.12
Tablet, Film-Coated; Oral; Levofloxacin Hemihydrate 500 mg (Tecnofarma)
Tablet, Film-Coated; Oral; Levofloxacin Hemihydrate 750 mg (Tecnofarma)
Tablets, Film-Coated; Oral; Levofloxacin Hemihydrate 500 mg (Tecnofarma)
Tablets, Film-Coated; Oral; Levofloxacin Hemihydrate 750 mg (Tecnofarma)
50 mg x 100 mL x 200ml (Novagen Pharmaceuticals)$ 1.14
Novaflox IV 50 mg Injection (Novagen Pharmaceuticals)$ 1.14
Novaflox IV 50mg x 100mL INJ / 200ml (Novagen Pharmaceuticals)$ 1.14
NOVAFLOX IV inj 50 mg x 100 mL x 200ml (Novagen Pharmaceuticals)$ 1.14
Novaflox IV 50mg x 100mL INJ / 200ml (Novagen Pharmaceuticals)$ 1.14
Novaflox OZ 250+500 Tablet (Novagen Pharmaceuticals)$ 0.11
Tablet; Oral; Levofloxacin Hemihydrate 250 mg
Tablet; Oral; Levofloxacin Hemihydrate 500 mg
Tablet; Oral; Levofloxacin Hemihydrate 750 mg
Tablets; Oral; Levofloxacin Hemihydrate 250 mg
Tablets; Oral; Levofloxacin Hemihydrate 500 mg

References

  1. DailyMed. "LEVOFLOXACIN: DailyMed provides trustworthy information about marketed drugs in the United States. DailyMed is the official provider of FDA label information (package inserts).". https://dailymed.nlm.nih.gov/dailyme... (accessed September 17, 2018).
  2. PubChem. "LEVOFLOXACIN". https://pubchem.ncbi.nlm.nih.gov/com... (accessed September 17, 2018).
  3. DrugBank. "LEVOFLOXACIN". http://www.drugbank.ca/drugs/DB01137 (accessed September 17, 2018).

Reviews

The results of a survey conducted on ndrugs.com for Neofloxacin are given in detail below. The results of the survey conducted are based on the impressions and views of the website users and consumers taking Neofloxacin. We implore you to kindly base your medical condition or therapeutic choices on the result or test conducted by a physician or licensed medical practitioners.

User reports

Consumer reported useful

No survey data has been collected yet


1 consumer reported price estimates

Was the price you paid to purchase the drug reasonable? Did you feel it was expensive?
The below mentioned numbers have been reported by ndrugs.com website users about whether the Neofloxacin drug is expensive or inexpensive. There is a mixed opinion among users. The rating about the cost of the drug depends on factors like which brand drug the patient purchased, how effective it was for the price paid, the country or place the drug is marketed, and the economic condition of the patient. The users who feel the drug is expensive can look for an alternative brand drug or a generic drug to save the cost.
Users%
Not expensive1
100.0%


2 consumers reported time for results

To what extent do I have to use Neofloxacin before I begin to see changes in my health conditions?
As part of the reports released by ndrugs.com website users, it takes 5 days and a few days before you notice an improvement in your health conditions.
Please note, it doesn't mean you will start to notice such health improvement in the same time frame as other users. There are many factors to consider, and we implore you to visit your doctor to know how long before you can see improvements in your health while taking Neofloxacin. To get the time effectiveness of using Neofloxacin drug by other patients, please click here.
Users%
5 days1
50.0%
1 day1
50.0%


1 consumer reported age

Users%
16-291
100.0%


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