Allergic Rhinitis (Hay Fever) – Treatment and Medicines
Allergic rhinitis or hay fever-
It is an irritation caused by a stimulus.
It is irritation and inflammation in the nose.
The tiny particles are breathed.
They irritate the inner nose lining, causing a flare reaction.
It releases histamine.
What are the Hay fever symptoms?
- Stuffy nose /runny nose
- Sneezing
- Itchiness in nose and eyes
- Mucus falling in the throat
- Tiredness
- Sinus pressures
What are the types of rhinitis?
Allergic rhinitis – It is nasal inflammation triggered by allergens.
Non-allergic rhinitis- It is triggered by weather changes, spicy foods, and strong smells.
Infectious rhinitis – It is caused by viral infections.
Is hay fever a real fever?
It is called hay fever because the allergy occurs due to hay.
Pollen, dust, etc. It does not cause fever directly.
The fever is caused by infection or cold, etc.
Difference between cold and hay fever-
Cold /Flu is an infection caused by a virus.
Hay fever is caused by an allergic reaction.
The allergy lasts until the allergen is in the environment.
It usually happens in the season of the pollen grains.
Allergic rhinitis /hay fever medicines-
Antihistamines –
They block the histamine receptors.
Histamine is released by the body (due to an allergy).
- Cetirizine
- Fexofenadine
- Loratadine
Nasal corticosteroids-
They help manage moderate to severe rhinitis.
They work directly into the nose.
It reduces nasal inflammation or swelling and mucus.
- Fluticasone propionate
- Budesonide
Decongestants –
These thin down the viscous mucus.
Mucus is excessively produced due to allergy.
- Pseudoephedrine
- Oxymetazoline
Leukotriene inhibitors-
These block the nasal inflammation.
- Montelukast
- Zafirlukast
How to prevent allergic rhinitis?
- Identify the triggers.
- Minimizing exposure.
- Keep the windows closed.
- Practice daily saline irrigation.
- Use intranasal corticosteroids.
- Practice cleaning habits
- Avoid smoking
- Wear sunglasses
- Avoid contact with pets
Allergic rhinitis can induce an asthma flare. How?
Rhinitis irritates the nose and eyes.
It affects the airway system.
The air is inhaled through the mouth.
The air is not warmed in the lungs and irritates the bronchi.
It may cause inflammation of the airway system.
It can cause an allergic flare.
The Third–party pharmaceutical manufacturer and the leading distributor-
Aprazer Healthcare is a global pharmaceutical manufacturer company.
We manufacture a range of global quality products.
Our product portfolio includes a wide range of drugs.
- Anti-Histamines
- Anti-Allergic & Common Cold Combinations
We are WHO –GMP certified and globally recognized.
Accredited by the EU-GMP, we are the leading drug suppliers to the Middle East markets.
Chemotherapy vs Targeted Therapy: Which is Better?
Chemotherapy and targeted therapy form the base of cancer treatment.
These are the systemic anti- cancer therapies.
The toxic drug agent circulates through the bloodstream.
Targeted therapy is precision drug therapy.
It targets the tumor site and the cancer cells.
It is used for specific genetic mutations.
It offers fewer side effects.
Chemotherapy drugs equally affect healthy/cancerous cells.
It is highly effective for fast-growing cancers.
It offers more severe side effects.
Chemotherapy and its uses-
These are the cytotoxic agents that kill the rapidly dividing cells, damaging the DNA.
The primary goal of using chemotherapy drugs is-
- Eliminate the cancer cells
- Prevent the spread of cancer cells to other organs
- Prevent recurrence of cancer
Chemotherapy is exclusively used in –
- Acute leukemia
- Aggressive lymphomas
- Small cell lung cancers
- Triple–negative breast cancer
Targeted therapy and its uses-
These are the cytotoxic drugs that target specific enzymes in cancer cells.
These target the cancer cell cycle.
The primary therapeutic goal of using targeted therapy drugs is-
- Starving the tumor cells
- Blocking the growth signals
- Enhancing the immune system
- Deliver targeted destruction
It is exclusively used in –
- Non-small cell lung cancer
- HER2-positive cancers
- BRCA1/BRCA2 reproductive system cancers
- Myeloid leukemia
Benefits and side effects of chemotherapy-
These offer broader protection.
These are widely used for –
- Fast-growing tumors
- Widespread cancers
- Highly mutating cancer cells
Common side effects include –
- Weakness
- Hair loss
- Bone marrow suppression
- Digestive issues
- Mouth ulcers
- Nerve damage
- Chemo brain
Benefits and side effects of Targeted therapy-
Targeted therapy drugs are used to target specific enzymes.
They are widely used to target –
- Localized tumors
- Specific mutations in the cancer
- Specific stage of the cancer
The common side effects include –
- Skin /nail changes
- Fatigue
- Diarrhea
- High Blood pressure
- Liver impairment
- Delayed wound healing
Which are the chemotherapy drugs?
- Cisplatin- Cycokast-50
- Capecitabine – Capekast
- Paclitaxel – Paclikast 260
- Doxorubicin – Dorucin
- Etoposide – Posiact
Which are the targeted therapy drugs?
- Imatinib – Imatikast 500
- Dasatinib – Dasakast 70
- Olaparib – Olabir
Which is the largest oncology medicine manufacturer?
Aprazer Healthcare is the leading anticancer drug manufacturer.
We are a global pharmaceutical company, specializing in manufacturing oncology orals and oncology injectables.
We are the top exporters of oncology medicine worldwide.
Accredited by the global health authorities, we manufacture top-quality anticancer drugs accepted and preferred worldwide.
What is Pharmaceutical Contract Manufacturing? A Complete Guide
It is the manufacturing of drugs for a company by an external party.
In this, the drugs are not manufactured by the owner company but are manufactured by another company.
The manufacturer company holds global licenses.
It ensures quality and regulatory compliance.
The owner holds the right to sell and market the products.
What is a Contract Development and Manufacturing Organization (CDMO)?
It is the manufacturing process from drug discovery to finished dosage formulation.
It involves a rigorous research and drug development process.
It includes the clinical trial process/ complete drug design.
The benefits of contract pharmaceutical manufacturing for global exporters-
Contract manufacturing helps global exporters save the cost of production.
- Eliminates the need for heavy investments
- It reduces regulatory burdens
- It leads to faster market access.
- Scalable production
How to select the best pharmaceutical contract manufacturer?
Making informed decisions fixes the need and alleviates unnecessary uncertainties.
Manufacturing Infrastructure-
The manufacturer must implement advanced manufacturing processes.
- In-house laboratories
- Advanced instruments
- Automated systems
- Sterility and containment facilities
- Qualified utilities
Regulatory compliance-
The exporters must ensure the regulatory-compliant manufacturing facilities.
The manufacturing unit must be WHO-GMP and ISO compliant.
For marketing products in strict markets, the manufacturers must hold country-specific regulatory certifications.
Quality Assurance –
The manufacturer must ensure strict regulatory adherence.
They must be able to provide-
- Batch analysis certificates
- Real-time stability testing data
- Ensure batch consistency
- Raw material quality
Manufacturing capabilities /capacity –
The dedicated facilities for toxic drug manufacturing.
Sterility and containment procedures.
The company must be able to manufacture advanced dosage formulations.
Sterile injectables, orals, and solid dosage forms.
Understand the capacity or the volume of manufacturing.
Confidentiality –
The manufacturing company must protect the proprietary rights of the owner company.
It must preserve the formula and the brand rights of the company.
Supply chain Efficiency –
- Proper logistic management
- Traceable supply chain
- Integrated cold chain
Transparency –
The manufacturer must manage transparency at all manufacturing steps.
From procuring raw material, raw material quality, and finished product quality, the supply chain must be transparent and documented.
Affordability without compromising quality –
The manufacturer must balance affordability and quality.
Global standard products must be manufactured without compromising quality.
Implementing new technology and automated processes maintains quality and also minimizes wastage.
Which is the globally recognized pharmaceutical contract manufacturer from India?
Aprazer Healthcare is a renowned pharmaceutical contract manufacturer from India.
We are built on a long-standing reputation of zero non-compliant audit history.
Our manufacturing unit adheres to WHO-GMP /EU-GMP standards.
Leveraging advanced technology, we are capable of manufacturing a comprehensive drug class.
Our extensive product portfolio spans –
Our core values that make us the leaders in contract drug manufacturing-
- Cost transparency
- Global compliance
- Fair MOQs
- Consistent quality
- Robust costumer services
- Regulatory expertise
Tranexamic Acid (TXA) – From Trauma Management to Heavy Period Relief
Tranexamic acid is a synthetic derivative.
It stops the excessive bleeding.
It prevents the dissolution of the blood clot.
It is an antifibrinolytic agent.
What is Tranexamic Acid (TXA) tablet used for?
It is widely used in surgical and medical conditions.
It inhibits the breakdown of the clot.
It prevents blood loss during –
- Heavy menstrual /postpartum bleeding
- Blood loss during surgery /trauma
- Dental procedures
- Nose bleeds
Tranexamic acid working –
It inhibits the plasmin enzyme.
Plasmin helps dissolve the clots.
Blocking the enzyme promotes clot formation.
It slows down bleeding.
Clot formation prevents blood loss.
Tranexamic acid use in trauma /surgery-
Tranexamic acid is widely used in trauma or hemorrhage.
It inhibits clot breakdown. It stops excessive bleeding.
It is given intravenously during accidents or traumatic hemorrhage.
It minimizes postoperative and intraoperative blood loss.
It is applied topically at the surgical site.
It helps reduce bruising and swelling.
The role of Tranexamic acid in period management (Menorrhagia)-
It is widely prescribed to manage heavy bleeding.
It slows down the breakdown of the clots.
It prevents excessive blood loss.
It is a non-hormone treatment.
It does not alter the hormones or the menstrual cycle.
Tranexamic acid use for skin issues-
Topical Tranexamic acid is widely applied to harness its anti-inflammatory properties.
Tranexamic acid blocks the pathway of pigmentation.
It is widely used to treat –
- Skin pigmentation
- Melasma
- Skin discoloration
It brightens the skin.
It minimizes dark sunspots/age spots on the skin.
Does tranexamic acid tablet relieve pain during periods?
Tranexamic acid does not help manage pain during periods.
It just prevents heavy bleeding and blood loss.
Tranexamic acid side effects –
The common side effects include-
- Headache
- Nasal congestion
- Muscle pain, joint pain
- Nausea
- Diarrhea
- Severe weakness
Serious side effects –
- Blood clot in the lungs, arms, etc.
- Trouble breathing
- Blurred vision
- Severe allergic rashes
- Stroke /heart issue
The third-party pharmaceutical manufacturer – A global export partner
Aprazer Healthcare is a pharmaceutical manufacturing company.
We manufacture a diverse range of life-saving medicines.
We are a trusted third-party drug manufacturer and exporter.
Our product portfolio includes-
We are a leading pharmaceutical company trusted by global exporters.
We export high-quality products to countries in Asia, Africa, and America.
Which is The Top Anti-Infective Drug Manufacturer in India?
Aprazer Healthcare manufactures a comprehensive range of anti-infective drugs.
Leveraging modern infrastructure, Aprazer Healthcare specializes in manufacturing complex dosage formulations.
We manufacture specialized dosage forms including all types of tablets and capsules.
Our extensive anti-infective product portfolio includes-
- Antibiotic combinations
- Antifungal drugs
- Antiviral drugs
- Anthelmintic drugs
Our flagship products include-
- Apraketo – Ketoconazole tablets
- Azithrokast 500– Azithromycin 500mg
- Ciprokast 500 – Ciprofloxacin 500mg
- Zerquan – Praziquantel
Manufacturing a complete range of antiviral drugs, Aprazer Healthcare is the leading manufacturer of –
- Antiretroviral combinations for HIV.
- Hepatitis B antivirals
- DDAs for Hepatitis C
Aprazer Healthcare is the leading contract drug manufacturing organization for anti-infective drugs. Why?
Regulatory compliance –
WHO-GMP and EU-GMP certified manufacturing units.
We have a long track record of manufacturing global quality drugs.
Our regulatory expertise, easily navigate export challenges.
Quality Assurance –
Adherence to regulatory standards, maintaining sterility and precision.
- Advanced air-handling systems
- Separate blocks for beta-lactam antibiotics.
- Environmental controls
- Uniformity of content
- Precise dose formulations
- In-house quality checks
- Pharmaco-vigilance and data integration.
Robust distribution network-
Aprazer Healthcare is the top supplier of anti-infective drugs in America, Africa, and Asia.
From procuring raw material to end-mile distribution, we have a transparent supply chain.
- Authentic supply logistics
- Cold chain supply
Extensive product portfolio – our widest portfolio includes all antibiotics and antivirals.
Crisis resilience – we remain crisis-ready in manufacturing large-scale anti-infective during an epidemic.
Scalable production – we are capable of manufacturing large-scale and small-scale batches.
Cost–effective manufacturing – Leveraging advanced technology and automated systems, we focus on preventing wastage and lowering production costs.
Why is precision required in manufacturing anti-infective drugs?
Unlike other generic formulations, anti-infective drugs need precise doses.
These directly target the viable microbes.
Any fluctuation in dosage may lead to failure of treatment.
The low doses may not achieve the required efficacy.
Higher doses may lead to toxicity.
It also increases the risk of antimicrobial drug resistance.
Why complete a full course of antibiotic drugs?
Leaving the antibiotic course in the middle may lead to re-infection.
An incomplete course may not be effective in killing the complete bacterial count.
It also leads to drug resistance; the microbes mutate and may not respond to the same drug.
Why trust Aprazer Healthcare?
Aprazer Healthcare is a trusted contract pharmaceutical manufacturer.
Our core values of transparency/streamlined work processes define us as a trusted CMO from India for global brands.
Partner with Aprazer Healthcare-secure your effective drug supplies.
Thalassemia – Extending Beyond Its Regions
Thalassemia, known to be rare and inherited.
The number of cases is rapidly rising globally.
The countries of the Middle East, Southeast Asia, and the Mediterranean are called the “Thalassemia Belt”.
India, Thailand, etc., have the highest prevalence.
Europe and America no longer remain behind due to global migration and genetic exchange.
What is Thalassemia?
It is a disorder of the blood.
In this, the body declines to produce hemoglobin.
What are the causes of the rise in Thalassemia?
Inheritance of the defective gene-
It is the inheritance of a defective gene from the parents.
Genetic mutation –
It is in regions of malaria prevalence.
The gene gets mutated. It is a natural occurrence to prevent malaria.
Migration –
The migration to new places has led to the transfer of genetic factors.
Internal family marriages –
The culture of marrying close family members.
Both parents have similar genes.
The Rapidly Rising Thalassemia Can Be Curbed Through Informed Decisions
Genetic counseling and understanding the family history help identify new cases.
Thalassemia is an inherited disorder. The severity of the disease can be identified by genetic testing of the fetus.
Parents can make an informed decision about pregnancy-
- Use other methods through IVF
- It helps with early treatment
Aprazer Healthcare – Making Healthcare Accessible, Affordable, and Informed
Aprazer Healthcare is a top pharmaceutical manufacturer/exporter.
We manufacture the widest range of pharmaceutical products for the critical needs.
A complete range of medicines for rare diseases, chronic diseases, blood disorders, and
Supportive therapies for complicated health conditions.
We have a strong global presence in domestic and international markets.
We are a trusted Indian pharmaceutical company with top exports.
The Types of Thalassemia-
- Alpha thalassemia
- Beta thalassemia
Thalassemia symptoms-
It can be asymptomatic.
It can show mild to moderate symptoms.
- Anemia
- Fatigue
- Yellowish skin
- Difficulty in breathing
- Dizziness
- Fast heartbeat
In severe cases –
- Jaundice
- Inhibits growth in children
- Bone defects
- Swelling in the stomach
- delayed puberty
- enlarged spleen
What complications are caused by Thalassemia?
- Iron overload – Due to blood transfusion
- Severe anemia – reduced hemoglobin
- Enlarged spleen – compensatory effect of the body
Treatment for Thalassemia –
- Blood Transfusion –
It is the external administration of blood into the body.
- Iron chelation-
It is the condition in which excess iron is removed through chelation.
- Stem cell therapy-
The faulty blood cells are replaced with the healthy ones.
The new blood cells are produced.
Conclusion –
Though inherited, Thalassemia cases can be reduced through genetic awareness.
Sterile Manufacturing Process for Oncology Injectables
Oncology drugs are highly potent and cytotoxic in nature.
These require stringent quality controls and regulatory adherence.
Chemotherapy is usually given in the form of injectables or infusions.
What are sterile injectables?
Sterile injectables are drugs administered by injection.
They are sterile preparations, free from pyrogen or any other microorganism.
It includes –
- Intravenous injections
- IV infusions
- Intramuscular injection
- Subcutaneous injection
The need for sterility in Injectables-
The drugs are directly administered into the bloodstream.
They have rapid effects. These bypass the first-pass metabolism.
Any contamination may directly lead to severe health risks.
What are the benefits of injectables?
- These bypass the GIT.
- 100 percent bioavailability
- Rapid action
- No GIT side effects
What is the sterile manufacturing process for oncology injectables?
- Aseptic manufacturing –
The drugs are mixed or processed in sterile closed-loop conditions.
- Sterile raw material
- Pyrogen-free water
- Environmental controls
- Containment control
Personnel safety –
The working people must be protected from cytotoxic agents.
- Use protective gear and clothing.
- Air lock-lock systems
- Access restrictions
- Sterilization and filtration –
The products are filtered to remove particulate matter.
The glass vials are washed and depyrogenated.
Rubber stoppers are sterilized.
- Aseptic fill finish /lyophilisation-
The sterile liquid preparations are dispensed in sterile vials or containers in an aseptic chamber.
The injectable flow is unidirectional.
The filling process should be free from any contamination.
The heat-sensitive oncology drugs are half-stoppered in the vials.
These are transferred to freeze–dryers to remove water.
The aluminum seals are crimped onto the vials immediately removing from the freeze dryers.
The sealing must be done in protected air zones to prevent contamination.
- Quality control and inspection –
The vials are inspected for leaks or particulate matter.
Container closure integrity.
Sterility testing/bacterial endotoxin testing.
WHO – GMP Regulations for sterile injectable manufacturing
The GMP standards emphasized:
- Product quality
- Sterility control
- Manufacturing consistency
- Regulatory compliance
EU-GMP regulations for sterile injectable manufacturing
EU-GMP practices emphasize-
- Cleanroom classification
- Personnel controls
- Contamination prevention
- Environment monitoring
- Air barriers
Why choose Aprazer Healthcare for oncology injectables?
Aprazer Healthcare is the leading oncology injectable manufacturer.
We are global oncology drug exporters.
We are equipped with world-class infrastructure.
We are accepted and trusted due to our quality attributes-
- Global Manufacturing standards
- Rigorous quality controls
- Regulatory compliance
- Containment prevention
- Cost-efficient manufacturing
WHO-GMP/ EU-GMP: The Important Difference
It consists of the international /universal standards of product quality /safety.
It is the basic requirement for all manufacturers to implement GMP.
EU-GMP focuses on essential GMP controls along with country-specific regulations.
This includes additional regional regulatory qualifications.
WHO-GMP manufacturing –
It is the global authority that forms the backbone of the regulatory framework.
The core principles remain consistent across the globe.
It is a basic requirement that ensures product safety and quality.
The GMP goals include –
- Safeguards patient safety
- Ensures product quality
- It forms the base of regulatory approvals
- Reduces the risk of product recall.
EU-GMP manufacturing –
It is European Union Good Manufacturing Practices.
This includes the specifications for the sale of drugs in Europe.
Along with the basic GMP principles, EU-GMP includes variations in regulatory frameworks.
It is the difference in methodology –
- Variation in audits
- Documentation structure
- Quality systems
What are WHO-GMP regulations?
The GMP guidelines ensure consistent product quality in accordance with the intended use.
It includes-
- Process of manufacturing
- Raw material
- Training facilities
- Documentation
- Distribution
What are EU-GMP regulations?
These regulations apply to manufacturers, exporters, and distributors.
These are mandatory requirements for the sale of medicines in Europe.
These lay strong emphasis on –
- Pharmaceutical quality systems
- Risk management
- Documentation /traceability
- Trained professionals
Is the WHO-GMP standard of manufacturing enough for global export?
WHO-GMP is applicable in many countries.
However, the highly regulated market requires additional inspections and approvals.
The countries where only WHO-GMP is eligible –
It is highly beneficial for low-income countries, ensuring product quality.
It is acceptable in countries in Africa, the Middle East, and parts of Asia.
It also forms the basis of drug qualification by the UN and International health agencies.
The countries that require additional approvals –
The additional regulatory frameworks are required in –
UK, USA, and European markets.
These are the stringent markets.
They individually assess the manufacturing facilities.
They enforce distinct local documentation based on the region.
Which is the WHO-GMP /EU-GMP certified pharmaceutical manufacturer?
Aprazer Healthcare is the leading pharmaceutical company from India.
It specializes in manufacturing GMP-compliant drugs.
We are the leading drug supplier to the international market.
Our regulatory team has expertise in drug approvals in different targeted markets, technical standards, and documentation demands.
Implementing cutting–edge technical flow, our manufacturing units are compliant with EU regulatory norms, providing complete documentation and regulatory support.
Our fully automated systems hold a zero-tolerance stance on data gaps, favoring EU-GMP steep technological requirements.
WHO-GMP Standards for Oncology Drug Manufacturing
WHO establishes stringent parameters for manufacturing oncology medicines.
The anti-cancer drugs are highly toxic, potent medicines.
They are developed in controlled environments with safety parameters.
Facility design/containment systems –
Dedicated facilities-
These are separate blocks or rooms for manufacturing toxic drugs.
Dedicated blocks for multi-step processes like granulation, blending, and tableting.
- Segregated material flow
- Restricted access barrier system
- Air-lock systems between multi-chamber rooms.
- Air-tight architecture, sealed floors and roof
Air conditioning systems (HVAC) –
It is used for clean room standardization and environmental isolation.
- Maintaining pressure variants in toxic zones.
- HEPA filters for air filtration.
- Unidirectional airflow
- Temperature and humidity control
Personnel Safety –
The anticancer drugs are highly toxic and irreversibly damage living tissue.
The manufacturers must ensure high safety measures for the workers.
Cytotoxic drug handling training must be provided.
- Use of protective gear /garments
- Air borne drug /particulate matter monitoring.
- Decontamination facilities like dedicated shower or eye wash stations.
Validation process-
It ensures that each activity and process is under permissible limits.
- Equipment /instrument validation
- Operational validation
- Design validation
- Installation validation
- Performance validation
- Cleaning validation
Waste product management –
The residue of the oncology drugs is highly toxic.
WHO recommends safe disposal of toxic components.
- Separate in/out bags.
- Chemical treating systems
- Segregation for biological, hazardous, or general waste
- Fumigation exhausts to neutralize toxic vapors.
Why is a stringent regulatory framework required for oncology drug manufacturing?
The manufacturing process of oncology drugs demands high precision and sterility.
These are cytotoxic drugs.
These are lethal and directly kill viable cells.
Requirement for precision-
They have narrow safety margins.
Large doses damage the organs.
A lowered dose may lead to treatment failure.
Safety of personnel-
Spilling or touching the drug component may damage human cells.
It can cause serious complications.
Dedicated flow lines-
This prevents cross-contamination.
A trace of the cytotoxic drug clinging to the pipes may get incorporated into other medicines through the same pipeline.
The Air flow systems-
Any vapor or fumes of the toxic product in the air may lead to hazardous results when inhaled.
The particulate matter in the air may contaminate other general products.
Which is the leading WHO-GMP certified oncology medicine manufacturer?
Aprazer Healthcare is an oncology medicine manufacturer.
Globally recognized for manufacturing top quality pharmaceuticals, we are the leading oncology drug exporters.
We are trusted for our commitment to quality (WHO-GMP standards).
We manufacture a wide range of oncology drugs.
Oncology orals/Oncology injectable
Our flagship products include chemotherapy injectables-
- Carboplatin – Carbokast 150
- Cisplatin – Cycokast -50
- Cytarabine 500mg – Cytarzer 500
- Doxorubicin – Dorucin -10
WHO-GMP Certified Hepatitis Medicine Manufacturer and Exporter from India
It contributes to 22 % of the total supply of generic hepatitis medicines.
Despite the major supply, Hepatitis remains a global health crisis.
Global Burden and Treatment Gap
- More than 350 million people worldwide suffer from hepatitis infection.
- 1.3 million Deaths occur every year due to the severe lack of testing and treatment access.
- 1.1 million Deaths occur due to cirrhosis caused by untreated Hepatitis B.
- Fewer than 5 % of infected individuals receive the life-saving antiviral treatment.
The common hepatitis drugs exported from India
Hepatitis C medicines exported from India –
Sofosbuvir + Velpatasavir tablets – Velakast
Daclatasvir and Sofosbuvir Tablets – Sofokast Plus
Ledipasvir & Sofosbuvir Tablets- Ledikast
Daclatasvir Tablets- Dacikast
Ribavirin Capsules- Ribasure
Sofosbuvir Tablets – Sofokast
Hepatitis B medicines exported from India –
Tenofovir Alafenamide 25 mg tablet- Tafnext
Entecavir 1mg- Entekor-1
Tenofovir Disoproxil Fumarate Tablets- Tudobest
Why Aprazer Healthcare is the leading Hepatitis Medicine Manufacturer/exporter
World-class infrastructure-
Equipped with modern equipment and technology, we are capable of manufacturing advanced products.
The advanced manufacturing processes minimize wastage, leading to cost-effective manufacturing.
Regulatory compliance
Our manufacturing processes strictly adhere to WHO-GMP /EU-GMP regulations.
Robust Quality controls
We adhere to the global standards of manufacturing.
- Stringent quality control protocols
- In–house quality checks and controls
- In-house testing
Strong distribution network
We are globally present, supplying affordable standard-quality drugs.
- Cold chain delivery systems
- Traceable supply chain
- Authentic logistic support
Robust documentation support
Our team of experts offers end-to-end support in –
- Drug approvals
- CTD dossiers for pharmaceutical importers
- Custom and logistic documents
Extensive product portfolio –
We specialize in manufacturing antiviral combinations
Our product portfolio comprises a comprehensive range of –
Why is it important to treat Hepatitis timely?
The delayed /untreated hepatitis infection progresses to irreversible liver damage.
- It leads to liver scarring.
- increases the risk of liver cancer
- Increases the risk of spreading the virus
Which hepatitis infection is curable?
Hepatitis C is highly curable.
It is treated by direct-acting antivirals.
Hepatitis B is not curable.
It is managed and treated by antiviral combinations.
How do hepatitis medicines work?
Hepatitis C medicines target the proteins required for viral cell multiplication.
It stops cell multiplication, leading to elimination.
Hepatitis B suppresses the virus. It lowers the viral count.
It prevents liver scarring and improves immunity.
What are the hepatitis medicine side effects?
The common side effects include-
- Weakness
- Dizziness
- Headache
- Stomach ache
- Diarrhea
- Insomnia
Treat the lethal virus through the effective solution offered by Aprazer Healthcare.
Aprazer Healthcare, as the leading ( Hepatology medicine manufacturer) is the trusted hepatitis medicine exporter.
We are the top drug exporters to countries in
Asia, Africa, the Middle East, and America.
