Ceftrox

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Medically reviewed

Laura Arias

Last updated on 22/12/2025

This page provides general, reference-level information compiled from official medical sources. It is not a substitute for professional medical advice, diagnosis, or treatment. For decisions about your health, please consult a qualified healthcare professional.

Overview of Ceftrox

This section defines the fundamental identity, classification, and general purpose of the medicine Ceftrox (Ceftriaxone Sodium), rigorously adhering to factual accuracy and excluding details regarding dosage, specific treatments, safety profiles, or administration instructions.

Property Description
Active ingredient Ceftriaxone Sodium
Form Powder for injection (Parenteral formulation)
Pharmacological class Third-generation Cephalosporin, beta-lactam Antibiotic
Common use Systemic bacterial infections
Origin Semi-synthetic

What Type of Medicine is Ceftrox?

Ceftrox is a prescription-only, semi-synthetic medication classified as a beta-lactam antibiotic. Its primary function is to eliminate bacterial infections within the body, positioning it as a powerful anti-infective agent. The chemical origin of Ceftrox derives from Ceftriaxone Sodium, which is the single active pharmaceutical ingredient responsible for its efficacy. Ceftriaxone is characterized by its broad-spectrum activity against susceptible organisms.

Composition and Physical Form of Ceftrox

Ceftrox belongs to the third-generation cephalosporin class of antibiotics. Its physical form is a sterile powder for injection, not a tablet or capsule for oral consumption. This preparation is a parenteral formulation that requires reconstitution with a suitable diluent before being administered by a healthcare professional, typically via intramuscular (IM) or intravenous (IV) routes. Ceftriaxone is recognized as a broad-spectrum cephalosporin active against numerous bacterial species. Unlike oral antibiotics, this injectable form provides rapid therapeutic concentrations, which is a differentiating factor for managing acute, time-sensitive infections.

What is the General Purpose of Ceftriaxone Sodium?

The fundamental purpose of Ceftriaxone Sodium is to act as a bactericidal agent that directly destroys susceptible bacteria causing infection. This occurs because the compound interferes with the bacteria's ability to build and maintain their essential cell wall structure. This action establishes its role as a treatment option in acute medical scenarios where rapid elimination of the systemic bacterial pathogen is required. The use of Ceftrox is typically reserved for serious infections such as sepsis or meningitis, scenarios where its potency and broad coverage are vital.

Regulatory References

  1. Ceftriaxone Injection: MedlinePlus Drug Information

What side effects are possible with Ceftrox?

Possible Side Effects and Safety Information

The safety profile of Ceftrox (Ceftriaxone Sodium) is based on official government regulatory documents, which classify potential reactions by frequency and affected physiological systems.

Frequency-Classified Adverse Reactions

Adverse reactions are organized into frequency categories as defined by regulatory standards. Common reactions (occurring in 1 to 10 out of 100 people) include changes in blood counts, such as eosinophilia, leukopenia, and thrombocytopenia; diarrhoea; elevated hepatic enzyme values; and localized pain or reactions at the injection site. Uncommon effects include fungal infections, nausea, vomiting, itching (pruritus), headache, fever, and phlebitis following intravenous administration.

Systemic Safety Concerns

Adverse effects are officially grouped by System-Organ-Class, including disorders of the Blood and Lymphatic System, Gastrointestinal tract, Hepatobiliary system, and Skin and Subcutaneous Tissue.

Serious Adverse Reactions are explicitly documented in official labeling. These include rare but critical events such as severe Anaphylactic Reactions or Shock, Serious Cutaneous Adverse Reactions (like Stevens-Johnson Syndrome), and Pseudomembranous Colitis (a severe inflammation of the colon). The formation of gallbladder precipitates, known as Biliary Pseudolithiasis, is also a documented concern.

Regulatory Constraints

The medicine is officially contraindicated for concurrent intravenous co-administration with any calcium-containing solutions in all age groups due to the risk of precipitation. Furthermore, it is contraindicated in neonates with hyperbilirubinemia due to the documented risk of kernicterus. Some effects, like hypersensitivity, are noted to occur early (treatment initiation), while Clostridium difficile-associated diarrhoea may occur during or after treatment is complete.

Overdose and Emergency Response

Ceftrox Overdose and When to Seek Help

Official regulatory information specifies that an overdose of Ceftrox (Ceftriaxone Sodium) carries the documented risk of serious complications, requiring immediate medical attention. The most significant risks documented in the regulatory profile are the development of urolithiasis (kidney stones) and subsequent Post-Renal Acute Renal Failure (PARF). Other formally documented clinical manifestations of overdose include nausea, vomiting, and diarrhoea.


Required Emergency Actions

The requirement for urgent medical help is established by the potential for life-threatening outcomes, such as Acute Renal Failure. Management in an overdose situation is strictly limited to symptomatic and supportive treatment, as regulatory agencies explicitly state that no specific antidote is known for Ceftriaxone.


Procedural Limitations

It is officially documented that the drug’s concentrations cannot be significantly reduced by established removal procedures such as haemodialysis or peritoneal dialysis. Furthermore, for patients with severe renal and hepatic dysfunction, close monitoring for adverse effects is necessary to prevent toxicity associated with high drug exposure.

Therapeutic Uses of Ceftrox

What Ceftrox Treats: Main Uses and Benefits

Ceftrox is a key anti-infective agent generally utilized to help with serious bacterial infections, focusing on eliminating the pathogens responsible for acute illness and providing critical therapeutic support. Its use is commonly reserved for conditions where potent, broad-spectrum coverage is required.


The medication is applicable within clinical settings that involve acute or disruptive symptom patterns. It is used in situations involving certain distressing symptoms across critical domains, including septicemia, bacterial meningitis, severe pneumonia, pyelonephritis, bone and joint infections, and intra-abdominal infections. Ceftrox supports the patient during difficult episodes by easing distress and helping to halt the progression of illness.

It may assist with managing intense symptom clusters that appear suddenly, such as high fever, chills, severe headache, and profound systemic distress.

“Ceftrox is used to provide support that helps ease the overall symptom burden associated with the bacterial infection.”

Quick Fact: Support for Systemic Distress

Ceftrox is often used when symptoms intensify and supportive relief is needed, contributing to improved comfort during periods of heightened symptoms and assisting with maintaining functional stability.

Regulatory References

  1. NIH MedlinePlus Drug Information overview

Eligibility and Restrictions for Use

The eligibility profile for Ceftrox (Ceftriaxone Sodium) is strictly defined by official government regulatory labeling. The medicine is approved for standard use in adults and children 15 days of age and older. Use in older adults is also generally allowed without specific dose adjustment, provided there is no severe concurrent organ impairment.


Contraindications and Prohibitions

Ceftrox is contraindicated and must not be used in specific populations due to risks documented by regulatory authorities:

  • Patients with a known severe allergy or hypersensitivity to ceftriaxone or any other cephalosporin antibiotic.
  • Premature neonates (up to 41 weeks post-menstrual age) and hyperbilirubinemic neonates (le 28 days old).
  • Neonates (le 28 days) requiring intravenous solutions containing calcium.

Conditional and Restricted Use

Restrictions apply to patients with combined severe renal and hepatic impairment, where the maximum daily dosage must be limited. Use requires caution in patients with a history of non-severe penicillin allergy. During pregnancy, Ceftrox should be used only if clearly needed. It is generally considered acceptable, with caution, during lactation.

What should I know about interactions with other medicines?

Ceftrox (which contains the active ingredient cefuroxime or ceftriaxone, depending on the formulation) can interact with other medications, potentially altering its effects or increasing the risk of side effects. It is vital to inform your doctor or pharmacist of all prescription, non-prescription (over-the-counter) medicines, and herbal supplements you are currently taking.

Significant Interactions to Note

Interacting Medicine/Product Potential Effect Management
Calcium-containing IV solutions Formation of potentially dangerous precipitates (particles) in the blood, particularly in newborns and infants. Ceftriaxone formulations MUST NOT be mixed with or administered with calcium-containing solutions intravenously.
Oral Anticoagulants (e.g., Warfarin) Increased risk of bleeding due to effects on blood clotting. Requires close monitoring of Prothrombin Time (PT/INR) and possible dose adjustment of the anticoagulant.
Probenecid Can increase the concentration of Ceftrox (Cefuroxime/Ceftriaxone) in the body. May prolong the effect of the antibiotic, sometimes used deliberately.
Aminoglycoside antibiotics (e.g., Gentamicin) Possible increased risk of kidney damage (nephrotoxicity). Close monitoring of kidney function is recommended.
Oral Contraceptives May reduce the effectiveness of birth control pills. Use additional non-hormonal barrier contraception (e.g., condoms) during and for seven days after treatment.

It is generally safe to consume alcohol with some Ceftrox formulations (like Cefuroxime), but it is always best to consult your healthcare provider regarding alcohol consumption and any other substances while on treatment, especially as alcohol can worsen side effects like dizziness.

Mechanism of Action

How Ceftrox Works

Ceftrox (Ceftriaxone) is a bactericidal agent whose mechanism of action focuses exclusively on dismantling the structural integrity of susceptible bacteria. The molecule acts as a structural decoy that targets Penicillin-Binding Proteins ( PBPs)—enzymes essential for bacteria to finalize their cell wall construction. Ceftrox achieves a covalent and irreversible inhibition of these PBPs (specifically transpeptidases), thereby neutralizing the crucial biological machinery required for cross-linking the cell wall's peptidoglycan scaffolding.

This enzyme inhibition initiates a fatal mechanistic cascade: the cell wall is synthesized in a structurally defective state, leaving the cell unable to withstand its own high internal osmotic pressure. This compromised integrity triggers the activation of bacterial autolytic enzymes and results in the rapid lysis (rupture) of the cell. This destructive action leads to the reduction of the viable bacterial population, a primary physiological consequence of the mechanism. The effectiveness of this mechanism is constrained by bacterial resistance strategies such as the production of beta-lactamase enzymes and the alteration of PBP targets.

Dosage and Administration Information

How Ceftrox is Used: Administration and Usage

Ceftrox (Ceftriaxone Sodium) is a prescription medicine administered exclusively by a healthcare professional via the parenteral route—meaning it is given as an intravenous (IV) infusion or injection or by deep intramuscular (IM) injection.

Standard Dosing and Schedule

For adults, the typical daily dosage is 1 gram (g) to 2 g of ceftriaxone, administered once every 24 hours. For severe infections, the dose may be raised to a maximum of 4 g daily, which may be given as a single dose or divided into two equally split doses every 12 hours. For surgical use, a single 1 g dose is typically given intravenously shortly before the procedure.

Preparation and Delivery Rules

Ceftrox is supplied as a sterile powder that must be properly reconstituted before administration. A critical constraint is the prohibition of co-administration with calcium-containing IV solutions, including some nutritional fluids. Intravenous infusions must be administered slowly over a period of at least 30 minutes. For IM injection, reconstitution with 1% Lidocaine solution is a method used to minimize injection discomfort, but such a solution must never be used for the intravenous route.

Adjustments for Specific Populations

In older adults and patients with impaired renal (kidney) or hepatic (liver) function, no dosage adjustment is typically required for daily doses up to 2 g, provided the other organ function is satisfactory. However, in cases of severe impairment affecting both the kidneys and the liver, the total daily dose should generally not exceed 2 grams.

Recent Clinical Evidence

Research Evidence / Overview of Studies for Ceftrox (Ceftriaxone Sodium)


Evidence for Use in Severe Pneumonia (Community-Acquired)

Ceftrox was studied for use in people hospitalized with severe lung infections, known as community-acquired pneumonia. The research primarily consists of Randomized Controlled Trials (RCTs) and large-scale retrospective cohort studies, where researchers observed patient data over time. These studies focused on measuring patient status after treatment, including endpoints related to clinical status (such as the presence of fever and breathing difficulties), and tracking longer-term outcomes like mortality (death rate) at 30 and 90 days.

Studies observed patterns in patients who received Ceftrox, often in comparison with patients who received other established antibiotics in the study setting. However, data show patterns related to outcomes that varied somewhat depending on the specific dosing regimen used.


Evidence for Use in Bacterial Meningitis

Research has examined Ceftrox's use in individuals with serious infections of the lining surrounding the brain and spinal cord. The evidence base includes Randomized Controlled Trials (RCTs) and comprehensive systematic reviews that synthesize many trials together. Studies monitored outcomes such as patient survival rate and long-term outcomes, including complications like neurological impairment (problems with the brain or nervous system). The studies were evaluated in both Adults and the Pediatric population (children).

Studies reported measurements of success based on whether the infection-causing bacteria were eradicated from the spinal fluid and measured long-term outcomes, including complications. However, when comparing Ceftrox directly to every other antibiotic available, the evidence quality varies across studies and is sometimes rated as very low, largely due to sample sizes were modest in some specific comparative trials.


Research Gaps and Areas of Scientific Uncertainty

Scientific literature consistently identifies several areas where research is ongoing or evidence is limited for Ceftrox. One key area of continued exploration is determining the optimal dosing strategy for critically ill patients, as different dosages was observed in some studies with varying results.

Furthermore, as bacteria continue to develop defenses, research is constantly examining the impact of evolving antimicrobial resistance on Ceftrox's use for conditions like complicated urinary tract infections and bloodstream infections. The comparative evidence is lacking or limited in certainty when measuring Ceftrox against every alternative treatment for specific infections. This means that evidence highlights what is known—and what is still uncertain—about its use in varied clinical circumstances.

Key Studies & References

  1. Ceftriaxone combination therapy versus respiratory fluoroquinolone monotherapy for community-acquired pneumonia: A meta-analysis
  2. Evidence review for antibiotics for bacterial meningitis before or in the absence of identifying causative infecting organism in adults - NCBI Bookshelf
  3. Ceftriaxone treatment of complicated urinary tract infections as a risk factor for enterococcal re-infection and prolonged hospitalization: A 6-year retrospective study
  4. ceftriaxone sodium injection, powder, for solution - FDA/DailyMed
  5. Cephalosporins - StatPearls - NCBI Bookshelf (General Mechanisms/Coverage)

Frequently Asked Questions (FAQ)

Common questions about Ceftrox (FAQ)

Q: What is the main difference between Ceftrox and other antibiotics for similar infections?

A: Ceftrox (Ceftriaxone) is classified as a third-generation cephalosporin, which is a specific class of antibiotics. According to regulatory documents, this drug is described as a broad-spectrum agent, indicating its effectiveness against a wide variety of Gram-negative and some Gram-positive bacteria. Its official classification as a third-generation cephalosporin places it within a specific category of antibiotics.

Q: Is Ceftrox a type of penicillin?

A: Ceftrox (Ceftriaxone) is a cephalosporin antibiotic, which is chemically distinct from the penicillin family. Both belong to the larger group of beta-lactam antibiotics. Official warnings state that patients with a known hypersensitivity to penicillin or other beta-lactam agents are warned of a potential risk of cross-reaction with Ceftrox.

Q: Can Ceftrox cause long-term problems or just short-term side effects?

A: Official information lists adverse effects that are generally expected to resolve after the medication is discontinued. However, the regulatory warning states that serious and rare events, such as Clostridium difficile-associated diarrhea (CDAD), have been reported to occur during treatment or up to two months afterward. For very specific patient populations, like newborns, serious complications related to calcium precipitates have been noted in official documents.

Q: Can I take Ceftrox if I am allergic to sulfa drugs?

A: Official product information emphasizes that Ceftrox is contraindicated if a person is known to be allergic to ceftriaxone, any other cephalosporin, or has a history of a severe reaction to penicillin. Official warnings and contraindications do not specifically link Ceftrox use to sulfa drug allergies.

Q: What happens if you drink alcohol while taking Ceftrox?

A: Unlike some other antibiotics, the official product information for Ceftrox (Ceftriaxone) does not carry a general prohibition on alcohol consumption. However, the medication is associated with potential side effects like dizziness, and alcohol consumption may potentially worsen these effects.

Q: Are there any common foods or supplements that interact with Ceftrox?

A: Regulatory documents list key interactions with specific intravenous (IV) solutions and other medications. No common food or daily supplements are explicitly listed as having interactions. However, Ceftrox can affect the results of certain lab tests, including non-enzymatic urine glucose tests.

Q: Is Ceftrox considered a 'broad-spectrum' antibiotic?

A: Yes, Ceftrox (Ceftriaxone) is officially classified as a broad-spectrum, third-generation cephalosporin antibiotic. This classification indicates its expected effectiveness against a wide variety of different bacteria.

Q: Why does the drug information warn against driving or operating machinery while on Ceftrox?

A: Regulatory labels list side effects such as dizziness or headache as uncommon adverse reactions to Ceftrox. Because these effects may temporarily impact a person’s ability to concentrate, official product information includes a general caution regarding operating machinery or driving.

Q: Is it possible to become resistant to Ceftrox over time?

A: The mechanism of action section on the label acknowledges that its effectiveness is constrained by bacterial resistance strategies, such as the bacteria producing certain enzymes. Regulatory warnings also note the potential risk of developing drug-resistant bacteria with the use of Ceftrox and other antibacterial agents.

Q: Can Ceftrox be used to treat viral infections like the common cold?

A: Ceftrox is an antibacterial agent and is only indicated for the treatment of susceptible bacterial infections. According to regulatory warnings, it will not treat viral illnesses, such as the common cold or flu, and should not be used in such cases.

Q: What is the connection between Ceftrox and blood sugar levels?

A: Regulatory documents state that Ceftrox can interfere with certain medical tests, particularly non-enzymatic urine glucose tests, sometimes causing false-positive results. Official guidance suggests that patients with diabetes may need to discuss appropriate glucose testing methods with their healthcare provider.

Q: What are the most commonly reported side effects of Ceftrox?

A: Official product labeling lists several common adverse reactions, primarily including gastrointestinal effects and skin rash. The complete list is available in the 'Possible side effects and safety information' section.

Q: Can Ceftrox affect the results of lab tests?

A: Yes, official information indicates Ceftrox can interact with certain medical tests. This may include tests for blood clotting, blood cell disorders (like hemolytic anemia), galactosemia, and urine glucose levels, potentially leading to inaccurate results.

Q: Is Ceftrox used for skin infections?

A: Ceftrox is officially indicated for the treatment of various susceptible bacterial infections. Regulatory labels state that this range of uses may include skin and skin structure infections.

Q: Why might a person not be eligible to use Ceftrox?

A: A person is generally not eligible if they have a known allergy to ceftriaxone, any other cephalosporin, or have a history of a severe reaction to penicillin. Additionally, it is contraindicated in premature neonates and newborns who have high bilirubin levels or are receiving intravenous solutions containing calcium.

Q: Are there any documented cases of Ceftrox causing anxiety or mood changes?

A: While specific reports of anxiety or mood changes are not commonly listed, official documents do list some central nervous system effects such as headache, dizziness, and seizures as rare or uncommon adverse reactions. Reports of confusion or hallucinations have also been documented in the product information.

Q: What kind of infections is Ceftrox not effective against?

A: Ceftrox is ineffective against viral infections like the common cold or flu. It is also not effective against bacteria that have developed resistance mechanisms, such as those that produce specific beta-lactamase enzymes that can break down the antibiotic.

Q: Can Ceftrox make existing health conditions worse?

A: Official warnings advise caution for patients with a history of certain gastrointestinal diseases, specifically colitis. Regulatory information indicates that caution is necessary for patients with existing kidney or liver conditions.

Q: Is 'diarrhea' from Ceftrox just a normal side effect or something serious?

A: Diarrhea is a common side effect of Ceftrox. However, official warnings specify that diarrhea that is watery or bloody, or occurring with severe abdominal pain, may indicate a serious condition called C. difficile-associated diarrhea (CDAD).

Q: What population groups are usually excluded from Ceftrox treatment?

A: Ceftrox is generally excluded for use in premature neonates and newborns who have high bilirubin levels or are receiving intravenous solutions containing calcium. The medication is also excluded for anyone with a known severe allergy to cephalosporins or penicillins.

Q: Is Ceftrox effective for sinus infections?

A: Ceftrox is officially indicated for a range of susceptible bacterial infections. While it is sometimes studied or used for complicated respiratory infections, the regulatory label specifies its use based on the susceptible bacteria identified, rather than the specific common name of the infection.

Q: Can Ceftrox cause temporary changes in taste or smell?

A: Yes, official regulatory documents list a change in taste (dysgeusia) and loss of taste as rare side effects that have been reported with Ceftrox use.

Q: Is there a generic version of Ceftrox available?

A: The active ingredient in Ceftrox is Ceftriaxone Sodium. According to public health databases, this active ingredient is widely available as a generic medicine in various formulations for administration by a healthcare professional.

Q: How is Ceftrox different from medications that end in '-cillin'?

A: Ceftrox (Ceftriaxone) is classified as a cephalosporin, making it chemically different from medications that end in '-cillin' (penicillins). Both are types of beta-lactam antibiotics, but the structural difference is why official warnings require caution for those with a penicillin allergy.

Q: Do older adults react differently to Ceftrox compared to younger adults?

A: According to official regulatory documents, appropriate studies performed to date have generally not demonstrated age-specific problems that would limit the usefulness of Ceftrox in the elderly population. This suggests that the response is generally comparable.

Q: Does Ceftrox interact with common pain relievers like ibuprofen or aspirin?

A: Official documents caution that the concurrent use of Ceftrox with certain Non-Steroidal Anti-Inflammatory Drugs (NSAIDs) may increase the risk of kidney-related side effects. Common pain relievers like ibuprofen and aspirin fall into the NSAID category, warranting awareness of this potential interaction.

Q: What are the signs of a non-severe allergic reaction to Ceftrox?

A: Signs of a general or non-severe allergic reaction listed in official documents may include rash, hives (welts), or itching. Any sign of an allergic reaction should be noted.

Q: Why do some people experience yeast infections after taking Ceftrox?

A: Ceftrox, like all broad-spectrum antibiotics, targets susceptible bacteria, including the 'good' bacteria that normally help control the growth of fungi. According to official warnings, this imbalance can result in secondary infections, or 'superinfections,' often caused by organisms such as yeasts or fungi.

Q: Are there any long-term research studies about Ceftrox safety?

A: Yes, regulatory documents reference studies that track patient outcomes over various time periods, including 30 and 90 days following treatment. For severe infections, such as meningitis, research has also monitored long-term complications like neurological impairment.

Q: Is Ceftrox a commonly used antibiotic globally?

A: As a third-generation cephalosporin, Ceftrox (Ceftriaxone) is widely recognized and used globally. It is commonly utilized in hospital settings due to its documented broad spectrum of activity and relatively long duration of action.

Q: Can Ceftrox be used to prevent an infection before surgery?

A: Yes, Ceftrox is officially indicated in regulatory documents for surgical prophylaxis. This means it is used to prevent potential bacterial infections associated with certain types of surgical procedures.

Q: Can the effectiveness of Ceftrox be reduced by other medications?

A: Yes, official product information indicates that Ceftrox may adversely affect the efficacy of oral hormonal contraceptives (birth control pills). The label advises using supplementary non-hormonal barrier contraception.

Q: Is Ceftrox safe to use during pregnancy?

A: The definitive safety of Ceftrox in human pregnancy has not been definitively established. Therefore, official documents state that the medication should only be used during pregnancy if the potential benefits are considered to outweigh potential risks.

Q: What risks are associated with using Ceftrox while breastfeeding?

A: Official information indicates that only minimal amounts of Ceftrox are found in breast milk. While caution is advised, studies generally suggest the medication poses minimal risk to the infant when used during breastfeeding.

Q: Is there any research on Ceftrox's use in children?

A: Yes, Ceftrox is indicated for use in children for a number of specific infections. Regulatory documents reference studies that have been performed in the pediatric population, including for serious conditions such as bacterial meningitis.

Q: Why do official documents sometimes mention Ceftrox by a different name?

A: The name 'Ceftrox' is a placeholder brand name. Official documents frequently refer to the drug by its active ingredient, ceftriaxone sodium. Some clinical information may also reference cefuroxime, as both are cephalosporin antibiotics used for similar purposes.

Q: Does Ceftrox interact with birth control pills?

A: Official information states that Ceftrox may adversely affect the efficacy of oral hormonal contraceptives. The regulatory label states that supplementary non-hormonal barrier contraception may be necessary during treatment and for a period of seven days afterward.

How should Ceftrox be stored and disposed of?

Ceftrox (Ceftriaxone Sodium for Injection) must be stored and handled according to specific regulatory requirements to ensure product stability.

Storage Requirements

Condition Rule
Temperature (Powder) Store at Controlled Room Temperature (20 C to 25 C).
Protection Must be protected from light and kept in the outer carton.
Container Keep the container tightly closed.

Stability and Handling

The unreconstituted powder is stable until the labeled expiration date when stored correctly. Once reconstituted, the solution is stable for up to 72 hours when refrigerated (2 C to 8 C), but it must not be frozen. The medicine must be stored out of the sight and reach of children.

Disposal Instructions

Unused or expired Ceftrox must be disposed of according to local requirements. The medicine must not be discarded via wastewater or household waste.

Attention! Always consult to a doctor or pharmacist before using pills or medicines.

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