Fexofenadine (Telfast, Allegra) is a second-generation antihistamine that is used to treat patients with symptoms of allergy such as flu, sneezing, itching, and urticaria.
Fexofenadine (Telfast) Uses:
-
Upper respiratory allergies:
- Relief from hay fever or other upper respiratory allergens that causes runny noses, throat irritation, and/or itchy, watery eyes.
-
Off Label Use of Fexofenadine in Adults:
- Chronic idiopathic urticaria
Also Read: Loratadine (Alavert); Use, Side effects, Dosage
Fexofenadine (Telfast) Dose in Adults
Fexofenadine (Telfast) Dose in the treatment of Upper respiratory allergies: Oral:
- Formulations for use twice daily: 60 mg per 12 hours (up to 120 mg per day).
- Formulations to be taken once daily: 180 mg once daily (up to 180 mg per day).
Fexofenadine (Telfast) Dose in the treatment of Chronic idiopathic urticaria (off-label):
- Oral: 180 mg once in a day or
- 60 mg twice a day
- Range: 20 to 240 mg two times in day.
Fexofenadine (Telfast) Dose in Children
Fexofenadine (Telfast) Dose in the treatment of Allergic symptoms/rhinitis: Oral:
-
Infants 6 months or more than 6 months and <10.5 kg:
- Oral suspension: 15 mg twice in a day.
- Dosing from a safety and tolerability study of infants with allergic rhinitis (n=58; mean age: 8.8 ± 1.6 months); adverse events were similar compared to placebo.
- Note: Five patients received 30 mg twice daily, which also had similar adverse effects compared to placebo.
-
Children 2 years or less than 2 years and less than10.5 kg: Limited data available:
- Oral suspension: 15 to 30 mg two times a day.
- Dosing from a safety and tolerability study of patients with allergic rhinitis receiving fexofenadine 15 mg two times in a day (n= 27; mean age: 16.1 months) or fexofenadine 30 mg two times in a day(n=103; mean age: 17.9 ± 3.2 months) compared to placebo.
- Adverse events were similar between patients receiving fexofenadine and patients receiving placebo (Hampell 2007).
-
Children 2 to 11 years:
- Oral suspension or orally disintegrating tablet (ODT):
- 30 mg two times a day.
- Oral suspension or orally disintegrating tablet (ODT):
-
Children ≥12 years and Adolescents:
- Tablets, orally disintegrating tablet (ODT):
- 60 mg two times in a day.
- Extended-release tablet:
- 180 mg once in a day.
- Tablets, orally disintegrating tablet (ODT):
Fexofenadine (Telfast) Dose in the treatment of Chronic idiopathic urticaria:
Note: Dosing based on previous FDA approved manufacturer labeling (Allegra prescribing information 2007): Oral:
-
Infants ≥6 months to Children <2 years:
- Oral suspension: 15 mg two times in a day.
-
Children 2 to 11 years:
- Oral suspension or orally disintegrating tablet (ODT):
- 30 mg two times a day.
- Oral suspension or orally disintegrating tablet (ODT):
-
Children ≥12 years and Adolescents:
- Tablets, orally disintegrating tablet (ODT):
- 60 mg two times a day.
- Extended-release tablet:
- 180 mg once in a day.
- Tablets, orally disintegrating tablet (ODT):
Fexofenadine pregnancy Risk Category: C
- There is limited information available about the pregnancy use of fexofenadine.
- Other agents that have more information about their use during pregnancy are preferred when a second-generation antihistamine becomes necessary.
Fexofenadine use during breastfeeding:
- We have not found information specific to breastfeeding and fexofenadine.
- After breastfeeding mothers have given terfenadine to their parent compound, fexofenadine was added to breast milk.
- Breastfeeding women may need to be treated with antihistamines. Second-generation antihistamines are more suitable for this population.
- Breastfed infants who were exposed to antihistamines have reported irritability and drowsiness. Infants exposed to terfenadine, the parent compound of fexofenadine, reported only irritability.
- Second-generation antihistamines tend to be less sedating than their first-generation counterparts.
Fexofenadine (Telfast) Dose in Kidney Disease:
- No dosage adjustment provide, except following (Aronoff 2007):
- GFR >50 mL/minute:
- No dosage adjustment necessary for twice in a day dosing (ie, 60 mg every 12 hours).
- GFR 10 to 50 mL/minute:
- 12 to 24 hours dose is recommended.
- GFR <10 mL/minute:
- Every 24 hours dose is recomended.
- Intermittent hemodialysis or peritoneal dialysis:
- Recommended dose every 24 hours.
- Continuous renal replacement therapy (CRRT):
- 60 mg every 24 hours.
- GFR >50 mL/minute:
Fexofenadine (Telfast) Dose in Liver disease:
No dosage adjustments.
Common Side Effects of Fexofenadine (Telfast):
-
Central nervous system:
- Headache
-
Gastrointestinal:
- Vomiting
Less Common Side Effects of Fexofenadine (Telfast):
-
Central Nervous System:
- Fatigue
- Dizziness
- Drowsiness
- Pain
-
Gastrointestinal:
- Nausea
- Dyspepsia
- Diarrhea
-
Genitourinary:
- Dysmenorrhea
-
Infection:
- Viral Infection
-
Neuromuscular & Skeletal:
- Back Pain
- Limb Pain
- Myalgia
-
Otic:
- Otitis Media
-
Respiratory:
- Cough
- Rhinorrhea
- Upper Respiratory Tract Infection
-
Miscellaneous:
- Fever
Contraindications to Fexofenadine (Telfast):
OTC labeling
- Do not use this medication for self-medication if you have ever had an adverse reaction to fexofenadine or any other ingredient.
Warnings and precautions
-
Renal impairment
- Patients with impaired renal function should be cautious. Dosage adjustment may be necessary.
Fexofenadine: Drug Interaction
Note: Drug Interaction Categories:
- Risk Factor C: Monitor When Using Combination
- Risk Factor D: Consider Treatment Modification
- Risk Factor X: Avoid Concomitant Use
Risk Factor C (Monitor therapy) |
|
Acetylcholinesterase Inhibitors | May diminish the therapeutic effect of Anticholinergic Agents. Anticholinergic Agents may diminish the therapeutic effect of Acetylcholinesterase Inhibitors. |
Alcohol (Ethyl) | Alcohol's CNS depressing effect may be amplified by CNS depressants (Ethyl). |
Alizapride | CNS depressants may have an enhanced CNS depressant impact. |
Amantadine | May strengthen an anticholinergic agent's anticholinergic action. |
Amezinium | Antihistamines may intensify Amezinium's stimulant effects. |
Amphetamines | May lessen antihistamines' sedative effects. |
Anticholinergic Agents | Other anticholinergic agents' negative or hazardous effects might be amplified. |
Betahistine | Betahistine's therapeutic impact may be reduced by antihistamines. |
Botulinum Toxin-Containing Products | May strengthen an anticholinergic agent's anticholinergic action. |
Brexanolone | Brexanolone's CNS depressing effects may be amplified by other CNS depressants. |
Brimonidine (Topical) | May enhance the CNS depressant effect of CNS Depressants. |
Bromopride | May enhance the CNS depressant effect of CNS Depressants. |
Cannabidiol | May enhance the CNS depressant effect of CNS Depressants. |
Cannabis | May enhance the CNS depressant effect of CNS Depressants. |
Chloral Betaine | May enhance the adverse/toxic effect of Anticholinergic Agents. |
Chlorphenesin Carbamate | May enhance the adverse/toxic effect of CNS Depressants. |
CNS Depressants | May enhance the adverse/toxic effect of other CNS Depressants. |
Dimethindene (Topical) | May enhance the CNS depressant effect of CNS Depressants. |
Doxylamine | May enhance the CNS depressant effect of CNS Depressants. Management: The manufacturer of Diclegis (doxylamine/pyridoxine), intended for use in pregnancy, specifically states that use with other CNS depressants is not recommended. |
Dronabinol | May enhance the CNS depressant effect of CNS Depressants. |
Eltrombopag | May increase the serum concentration of OATP1B1/1B3 (SLCO1B1/1B3) Substrates. |
Erdafitinib | P-glycoprotein/ABCB1 Substrates serum levels can rise. |
Erythromycin (Systemic) | Fexofenadine serum concentration can rise. |
Esketamine | CNS depressants may have an enhanced CNS depressant impact. |
Gastrointestinal Agents (Prokinetic) | The therapeutic benefit of gastrointestinal agents may be diminished by anticholinergic agents (Prokinetic). |
Gemfibrozil | May raise the level of OATP1B1/1B3 (SLCO1B1/1B3) Substrates in the serum. Agents indicated as exceptions should be examined in separate drug interaction monographs. |
Glucagon | Anticholinergic drugs may make glucagon's harmful or toxic effects worse. Particularly, there may be a higher chance of unfavourable gastrointestinal consequences. |
Grapefruit Juice | Fexofenadine's serum concentration can drop. |
HydrOXYzine | CNS depressants may have an enhanced CNS depressant impact. |
Itopride | Itopride's therapeutic impact may be diminished by anticholinergic drugs. |
Itraconazole | Fexofenadine serum concentration can rise. |
Kava Kava | CNS depressants may have a stronger effect on the CNS. |
Ketoconazole (Systemic) | Fexofenadine serum concentration can rise. |
Lofexidine | CNS depressants may have an enhanced CNS depressant impact. Management: Separate drug interaction monographs go into further detail about the medications indicated as exceptions to this book. |
Lumacaftor | May lower the level of P-glycoprotein/ABCB1 Substrates in the serum. The serum concentration of P-glycoprotein/ABCB1 Substrates may rise when using lumacaftor. |
Magnesium Sulfate | CNS depressants may have an enhanced CNS depressant impact. |
MetyroSINE | The sedative effects of metyroSINE may be strengthened by CNS depressants. |
Mianserin | May strengthen an anticholinergic agent's anticholinergic action. |
Minocycline | CNS depressants may have an enhanced CNS depressant impact. |
Mirabegron | Anticholinergic drugs may make Mirabegron's harmful or hazardous effects worse. |
Mirtazapine | The CNS depressing action of mirtazapine may be enhanced by CNS depressants. |
Nabilone | CNS depressants may have an enhanced CNS depressant impact. |
Nitroglycerin | Nitroglycerin absorption may be decreased by anticholinergic agents. |
P-glycoprotein/ABCB1 Inducers | Anticholinergic medications specifically have the potential to impede or prevent the absorption of nitroglycerin by reducing the breakdown of sublingual nitroglycerin pills. |
P-glycoprotein/ABCB1 Inhibitors | May lower the level of Pglycoprotein/ABCB1 Substrates in the serum. P-glycoprotein inducers may also further restrict the distribution of p-glycoprotein substrates to particular cells, tissues, and organs that have high levels of p-glycoprotein (e.g., brain, T-lymphocytes, testes, etc.). |
Piribedil | Piribedil's CNS depressing effects may be enhanced by other CNS depressants. |
Pitolisant | Pitolisant's therapeutic effects may be lessened by antihistamines. |
Pramipexole | The sedative effects of pramipexole might be enhanced by CNS depressants. |
Ramosetron | Ramosetron's constipating effects may be enhanced by anticholinergic drugs. |
Ranolazine | P-glycoprotein/ABCB1 Substrates serum levels can rise. |
RifAMPin | Fexofenadine's serum concentration can drop. Fexofenadine's serum levels may rise in response to RifAMPin. |
ROPINIRole | The sedative effects of CNS depressants may increase those of ROPINIRole. |
Rotigotine | Rotigotine's sedative effects may be boosted by CNS depressants. |
Rufinamide | CNS depressants' harmful or toxic effects could be increased. Particularly, drowsiness and lightheadedness could be worsened. |
Selective Serotonin Reuptake Inhibitors | Selective serotonin reuptake inhibitors may have a worsened or more hazardous effect when taken with CNS depressants. Particularly, there may be an increased risk of psychomotor impairment. |
Teriflunomide | May raise the level of OATP1B1/1B3 (SLCO1B1/1B3) Substrates in the serum. |
Tetrahydrocannabinol | CNS depressants may have an enhanced CNS depressant impact. |
Tetrahydrocannabinol and Cannabidiol | May enhance the CNS depressant effect of CNS Depressants. |
Thiazide and Thiazide-Like Diuretics | Anticholinergic Agents may increase the serum concentration of Thiazide and Thiazide-Like Diuretics. |
Topiramate | Anticholinergic Agents may enhance the adverse/toxic effect of Topiramate. |
Trimeprazine | May enhance the CNS depressant effect of CNS Depressants. |
Verapamil | May increase the serum concentration of Fexofenadine. |
Risk Factor D (Consider therapy modification) |
|
Antacids | Fexofenadine's serum concentration can drop. Administration of fexofenadine and antacids containing aluminium or magnesium should be separated. Calcium carbonate, magnesium, and sodium bicarbonate are exceptions. |
BenzylpenicilloylPolylysine | Antihistamines may diminish the diagnostic effect of BenzylpenicilloylPolylysine. Management: Suspend systemic H1 antagonists for benzylpenicilloyl-polylysine skin testing and delay testing until systemic antihistaminic effects have dissipated. A histamine skin test may be used to assess persistent antihistaminic effects. |
Blonanserin | CNS Depressants may enhance the CNS depressant effect of Blonanserin. |
Buprenorphine | CNS Depressants may enhance the CNS depressant effect of Buprenorphine. Management: Consider reduced doses of other CNS depressants, and avoiding such drugs in patients at high risk of buprenorphine overuse/self-injection. Initiate buprenorphine patches (Butrans brand) at 5 mcg/hr in adults when used with other CNS depressants. |
Chlormethiazole | May enhance the CNS depressant effect of CNS Depressants. Management: Monitor closely for evidence of excessive CNS depression. The chlormethiazole labeling states that an appropriately reduced dose should be used if such a combination must be used. |
Droperidol | CNS depressants may have an enhanced CNS depressant impact. Consider lowering the dosage of droperidol or other CNS drugs (such as opioids or barbiturates) when they are used concurrently. In separate drug interaction monographs, exceptions to this monograph are covered in more detail. |
Flunitrazepam | CNS Depressants may enhance the CNS depressant effect of Flunitrazepam. |
Hyaluronidase | Antihistamines may diminish the therapeutic effect of Hyaluronidase. Management: Patients receiving antihistamines (particularly at larger doses) may not experience the desired clinical response to standard doses of hyaluronidase. Larger doses of hyaluronidase may be required. |
HYDROcodone | CNS Depressants may enhance the CNS depressant effect of HYDROcodone. Management: Avoid concomitant use of hydrocodone and benzodiazepines or other CNS depressants when possible. These agents should only be combined if alternative treatment options are inadequate. If combined, limit the dosages and duration of each drug. |
Methotrimeprazine | CNS Depressants may enhance the CNS depressant effect of Methotrimeprazine. Methotrimeprazine may enhance the CNS depressant effect of CNS Depressants. Management: Reduce adult dose of CNS depressant agents by 50% with initiation of concomitant methotrimeprazine therapy. Further CNS depressant dosage adjustments should be initiated only after clinically effective methotrimeprazine dose is established. |
Opioid Agonists | CNS Depressants may enhance the CNS depressant effect of Opioid Agonists. Management: Avoid concomitant use of opioid agonists and benzodiazepines or other CNS depressants when possible. These agents should only be combined if alternative treatment options are inadequate. If combined, limit the dosages and duration of each drug. |
OxyCODONE | CNS Depressants may enhance the CNS depressant effect of OxyCODONE. Management: Avoid concomitant use of oxycodone and benzodiazepines or other CNS depressants when possible. These agents should only be combined if alternative treatment options are inadequate. If combined, limit the dosages and duration of each drug. |
Perampanel | May enhance the CNS depressant effect of CNS Depressants. Management: Patients taking perampanel with any other drug that has CNS depressant activities should avoid complex and high-risk activities, particularly those such as driving that require alertness and coordination, until they have experience using the combination. |
Pramlintide | May enhance the anticholinergic effect of Anticholinergic Agents. These effects are specific to the GI tract. |
Secretin | Anticholinergic Agents may diminish the therapeutic effect of Secretin. Management: Avoid concomitant use of anticholinergic agents and secretin. Discontinue anticholinergic agents at least 5 half-lives prior to administration of secretin. |
Sodium Oxybate | May enhance the CNS depressant effect of CNS Depressants. Management: Consider alternatives to combined use. When combined use is needed, consider minimizing doses of one or more drugs. Use of sodium oxybate with alcohol or sedative hypnotics is contraindicated. |
Suvorexant | CNS Depressants may enhance the CNS depressant effect of Suvorexant. Management: Dose reduction of suvorexant and/or any other CNS depressant may be necessary. Use of suvorexant with alcohol is not recommended, and the use of suvorexant with any other drug to treat insomnia is not recommended. |
Tapentadol | May enhance the CNS depressant effect of CNS Depressants. Management: Avoid concomitant use of tapentadol and benzodiazepines or other CNS depressants when possible. These agents should only be combined if alternative treatment options are inadequate. If combined, limit the dosages and duration of each drug. |
Tolvaptan | May increase the serum concentration of OATP1B1/1B3 (SLCO1B1/1B3) Substrates. |
Zolpidem | CNS Depressants may enhance the CNS depressant effect of Zolpidem. Management: Reduce the Intermezzo brand sublingual zolpidem adult dose to 1.75 mg for men who are also receiving other CNS depressants. No such dose change is recommended for women. Avoid use with other CNS depressants at bedtime; avoid use with alcohol. |
Risk Factor X (Avoid combination) |
|
Aclidinium | May enhance the anticholinergic effect of Anticholinergic Agents. |
Azelastine (Nasal) | CNS Depressants may enhance the CNS depressant effect of Azelastine (Nasal). |
Bromperidol | May enhance the CNS depressant effect of CNS Depressants. |
Cimetropium | Anticholinergic Agents may enhance the anticholinergic effect of Cimetropium. |
Eluxadoline | Anticholinergic Agents may enhance the constipating effect of Eluxadoline. |
Glycopyrrolate (Oral Inhalation) | Anticholinergic Agents may enhance the anticholinergic effect of Glycopyrrolate (Oral Inhalation). |
Glycopyrronium (Topical) | May enhance the anticholinergic effect of Anticholinergic Agents. |
Ipratropium (Oral Inhalation) | May enhance the anticholinergic effect of Anticholinergic Agents. |
Levosulpiride | Anticholinergic Agents may diminish the therapeutic effect of Levosulpiride. |
Orphenadrine | CNS Depressants may enhance the CNS depressant effect of Orphenadrine. |
Oxatomide | May enhance the anticholinergic effect of Anticholinergic Agents. |
Oxomemazine | May enhance the CNS depressant effect of CNS Depressants. |
Paraldehyde | CNS Depressants may enhance the CNS depressant effect of Paraldehyde. |
Potassium Chloride | Anticholinergic Agents may enhance the ulcerogenic effect of Potassium Chloride. Management: Patients on drugs with substantial anticholinergic effects should avoid using any solid oral dosage form of potassium chloride. |
Potassium Citrate | Anticholinergic Agents may enhance the ulcerogenic effect of Potassium Citrate. |
Revefenacin | Anticholinergic Agents may enhance the anticholinergic effect of Revefenacin. |
Thalidomide | CNS Depressants may enhance the CNS depressant effect of Thalidomide. |
Tiotropium | Anticholinergic Agents may enhance the anticholinergic effect of Tiotropium. |
Umeclidinium | May enhance the anticholinergic effect of Anticholinergic Agents. |
Monitoring parameters:
Relief of symptoms
How to administer Fexofenadine (Telfast)?
Orally disintegrating tablet:
- Administer when fasting.
- The tablet will dissolve with or without water if you take it out of the individual blister and place it right away on your tongue (do not administer with fruit juices).
Oral suspension, tablet:
- Do not administer with fruit juices; always administer with water.
- Before use, thoroughly shake the suspension. Use the provided dosage cup exclusively for suspension.
Mechanism of action of Fexofenadine (Telfast):
- Terfenadine has an active metabolite called fexofenadine.
- The search for H-1 receptor sites on effector cells of the gastrointestinal tract, blood arteries, and respiratory tract involves a competition with histamine.
- Fexofenadine doesn't appear to significantly cross the blood-brain barrier, which translates in a lesser risk of sedation.
The onset of action:
- 2 hours
Duration of action:
- 24 hours
Absorption:
- Rapid
Protein binding:
- 60% to 70%;
- primarily albumin and alpha -acid glycoprotein
Metabolism:
- Minimal (hepatic: 5%); 3.6% converted into a methyl ester metabolite that is only present in faeces
Bioavailability:
- ~33 percent
Half-life elimination:
- 14.4 hours (or 72% longer in patients with severe renal impairment [CrCl 11 to 40 mL/minute]; mild to moderate renal impairment [CrCl 41 to 80 mL/minute] people).
Time to peak, serum:
- ODT:
-
- 2 hours (4 hours with high-fat meal);
-
- Tablet:
- ~2.6 hours.
- Suspension:
- ~1 hour
Excretion:
- Feces (80%) and urine (12%) as unchanged drug.
International Brand Names of Fexofenadine:
- Alertam
- Alexia
- Allegra
- Allegra 180
- Allegra Allergy
- Allegratab
- Allemax
- Allerex
- Altifex
- Altiva
- Avafast
- Bosnum
- Bosnum 180
- Delaxin
- Ewofex
- Exofen
- Fastel
- Fe Min
- Fenadex
- Fenadin
- Fenafex
- Fexet
- Fexodex
- Fexodine
- Fexofast
- Fexofen
- Fexon
- Allegra Allergy Childrens
- Allegra Allergy
- Allergy 24-HR
- Allergy Relief
- Fexofenadine HCl Childrens
- Mucinex Allergy
- Alagra
- Alanil
- Alerfedine
- Fexoral
- Fexotabs
- Fexotene
- Fexovid
- Fynadin
- Inflex
- Kofixir
- Nasaga
- Neofex
- Raltiva
- Rhinogan
- Ritch
- Sizzle
- SkyFexo
- Tefodine
- Telfast
- Telfast HD
- Telfast OD
- Telfast Oral Solution
- Telfor
- Ternafast
- Tocimat
- Tofexo
- Vifas
- Xadine
- Xergic
- Xofast
Fexofenadine Brand Names in Pakistan:
Fexofenadine Susp 30 Mg/5ml in Pakistan |
|
Fenadrin | Noa Hemis Pharmaceuticals |
Fexofast | Platinum Pharmaceuticals (Pvt.) Ltd. |
Fexofenadine 60 Mg Tablets in Pakistan |
|
Adine | Pfizer Laboratories Ltd. |
Afex | Shaheen Agencies |
Alergino | Saydon Pharmaceutical Industries (Pvt) Ltd. |
Aller | Lotus Pharmaceuticals (Pvt) Ltd |
Allerfedin | Heal Pharmaceuticals Pvt Ltd |
Allergofex | Leads Pharma (Pvt) Ltd |
Allergofex Plus | Leads Pharma (Pvt) Ltd |
Alofex | Derma Techno Pakistan |
Alrin | Consolidated Chemical Laboratories (Pvt) Ltd. |
Aspen | Zephyr Pharmatec (Pvt) Ltd. |
Cibler | Pakistan Pharmaceutical Products (Pvt) Ltd. |
Elergifen | Semos Pharmaceuticals (Pvt) Ltd. |
Epodin | Epoch Pharmaceutical |
Exit-D | Fozan Pharmaceuticals Industriers (Pvt) Ltd |
Exofen | Aries Pharmaceuticals (Pvt) Ltd |
Fanamed | Medicaids Pakistan (Pvt) Ltd. |
Fanasel | Hansel Pharmacueutical Pvt (Ltd) |
Fanoxin | Jawa Pharmaceuticals(Pvt) Ltd. |
Faxodine | Libra Pharmaceuticals (Pvt) Ltd |
Fekom | Karachi Chemical Industries |
Fenadex | Global Pharmaceuticals |
Fenix | Healthtek (Pvt) Ltd |
Fenofex | Geofman Pharmaceuticals |
Fenosaf | Saaaf Pharmaceuticals |
Fenoxy | Paramount Pharmaceuticals |
Fesjet | Tagma Pharma (Pvt) Ltd. |
Fexera | Medera Pharmaceuticals (Pvt) Ltd. |
Fexet | Getz Pharma Pakistan (Pvt) Ltd. |
Fexheal | Opal Laboratories (Pvt) Ltd. |
Fexigen | Genera Pharmaceuticals |
Fexigra | Danas Pharmaceuticals (Pvt) Ltd |
Fexine | Fynk Pharmaceuticals |
Fexo | Hilton Pharma (Pvt) Limited |
Fexocare | Adcare Pharma |
Fexocare | Aims Pharmaceuticals |
Fexodrine | Fassgen Pharmaceuticals |
Fexofast | Platinum Pharmaceuticals (Pvt.) Ltd. |
Fexofax | Alliance Pharmaceuticals (Pvt) Ltd. |
Fexokure | Kurative Pak (Pvt) Ltd |
Fexolyd | Zesion Pharmaceutical (Pvt) Ltd |
Fexoprime | Pearl Pharmaceuticals |
Fexotel-3h | Hamaz Pharmaceutical (Pvt) Ltd. |
Fexowan | Swan Pharmaceuticals(Pvt) Ltd |
Fifex | Shaigan Pharmaceuticals (Pvt) Ltd |
Fiofen | Schazoo Zaka |
Fixfast | Hygeia Pharmaceuticals |
G-Fast | Olive Laboratories |
Genfix | Genix Pharma (Pvt) Ltd |
Meadow | Macter International (Pvt) Ltd. |
Nexofen | Neo Medix |
Nifty | Shrooq Pharmaceuticals |
Novahist | Pacific Pharmaceuticals Ltd. |
Regofast | Regent Laboratories Ltd. |
Remast | Nexus Pharma (Pvt) Ltd |
Sb-Din | Unison Chemical Works |
Sizzle | Wilshire Laboratories (Pvt) Ltd. |
Sneez | Unimark Pharmaceuticals |
Softin-F | Welwrd Pharmaceuticals |
Telfast | Sanofi Aventis (Pakistan) Ltd. |
Tidin | Miracle Pharmaceuticals(Pvt) Ltd |
Tilast | Vega Pharmaceuticals Ltd. |
Unifenadine | Tg Pharma |
Vasofax | Dyson Research Laboratories |
Welfast | Webros Pharmaceuticals |
Xadine | Searle Pakistan (Pvt.) Ltd. |
Xfr | Elko Organization (Pvt) Ltd. |
Xofea | Epharm Laboratories |
Xofena | Rock Pharmaceuticals |
Fexofenadine 80 Mg Tablets in Pakistan |
|
Novahist | Pacific Pharmaceuticals Ltd. |
Fexofenadine 120 Mg Tablets in Pakistan |
|
Adine | Pfizer Laboratories Ltd. |
Afex | Shaheen Agencies |
Alerfex | Genome Pharmaceuticals (Pvt) Ltd |
Alergino | Saydon Pharmaceutical Industries (Pvt) Ltd. |
Allegra | Helix Pharma (Private) Limited |
Aller | Lotus Pharmaceuticals (Pvt) Ltd |
Allerfedin | Heal Pharmaceuticals Pvt Ltd |
Allergia | Mass Pharma (Private) Limited |
Allergofex | Leads Pharma (Pvt) Ltd |
Aloc | Bosch Pharmaceuticals (Pvt) Ltd. |
Alrin | Consolidated Chemical Laboratories (Pvt) Ltd. |
Aspen | Zephyr Pharmatec (Pvt) Ltd. |
Axifax | Axis Pharmaceuticals |
Axodine | Gray`S Pharmaceuticals |
Cibler | Pakistan Pharmaceutical Products (Pvt) Ltd. |
Elergifen | Semos Pharmaceuticals (Pvt) Ltd. |
Exit | Fozan Pharmaceuticals Industriers (Pvt) Ltd |
Exofen | Aries Pharmaceuticals (Pvt) Ltd |
Fanasel | Hansel Pharmacueutical Pvt (Ltd) |
Fanoxin | Jawa Pharmaceuticals(Pvt) Ltd. |
Faxheal | Venture Chemical & Pharmaceuticals (Pvt) Ltd. |
Faxodine | Libra Pharmaceuticals (Pvt) Ltd |
Fekom | Karachi Chemical Industries |
Fenadex | Global Pharmaceuticals |
Fenadrin | Noa Hemis Pharmaceuticals |
Fendin | Pulse Pharmaceuticals |
Fendina | Highnoon Laboratories Ltd. |
Fenix | Healthtek (Pvt) Ltd |
Fenofex | Geofman Pharmaceuticals |
Fenoxy | Paramount Pharmaceuticals |
Fesjet | Tagma Pharma (Pvt) Ltd. |
Fexera | Medera Pharmaceuticals (Pvt) Ltd. |
Fexet | Getz Pharma Pakistan (Pvt) Ltd. |
Fexheal | Opal Laboratories (Pvt) Ltd. |
Fexigen | Genera Pharmaceuticals |
Fexigra | Danas Pharmaceuticals (Pvt) Ltd |
Fexine | Fynk Pharmaceuticals |
Fexinol | Martin Dow Pharmaceuticals (Pak) Ltd. |
Fexo | Hilton Pharma (Pvt) Limited |
Fexocare | Adcare Pharma |
Fexocare | Aims Pharmaceuticals |
Fexofast | Platinum Pharmaceuticals (Pvt.) Ltd. |
Fexofax | Alliance Pharmaceuticals (Pvt) Ltd. |
Fexofin | Bio Labs (Pvt) Ltd. |
Fexokure | Kurative Pak (Pvt) Ltd |
Fexolyd | Zesion Pharmaceutical (Pvt) Ltd |
Fexoprime | Pearl Pharmaceuticals |
Fexorex | Biorex Pharmaceuticals |
Fexosneez | Fassgen Pharmaceuticals |
Fexosure | Medisure Laboratories Pakistan (Pvt.) Ltd. |
Fexota | Orta Labs. (Pvt) Ltd. |
Fexotel-3h | Hamaz Pharmaceutical (Pvt) Ltd. |
Fexowan | Swan Pharmaceuticals(Pvt) Ltd |
Fexsel | Selmore Agencies |
Fifex | Shaigan Pharmaceuticals (Pvt) Ltd |
Fiofen | Schazoo Zaka |
Fixfast | Hygeia Pharmaceuticals |
Genfix | Genix Pharma (Pvt) Ltd |
Geridin | Ferroza International Pharmaceuticals (Pvt) Ltd. |
Hasty | Phar-Man Laboratories |
Histafex | Popular Chemical Works (Pvt) Ltd. |
Kovence | Medisure Laboratories Pakistan (Pvt.) Ltd. |
Makfex | Makson Pharmaceuticals |
Meadow | Macter International (Pvt) Ltd. |
Mexodine | Mediate Pharmaceuticals (Pvt) Ltd |
Nexofen | Neo Medix |
Nifty | Shrooq Pharmaceuticals |
Novahist | Pacific Pharmaceuticals Ltd. |
Ofenad | Rasco Pharma |
Plexid | Atco Laboratories Limited |
Regofast | Regent Laboratories Ltd. |
Remast | Nexus Pharma (Pvt) Ltd |
Revofex | Kaizen Pharmaceuticals Pvt Ltd. |
Sapifex | Sapient Pharma |
Sizzle | Wilshire Laboratories (Pvt) Ltd. |
Sneez | Unimark Pharmaceuticals |
Softin-F | Welwrd Pharmaceuticals |
Tansidin | Tansy Pharmaceuticals (Pvt) Ltd. |
Tefend | Glitz Pharma |
Telfast | Sanofi Aventis (Pakistan) Ltd. |
Telfex | Polyfine Chempharma (Pvt) Ltd. |
Telwin | Wns Field Pharmaceuticals |
Tidin | Miracle Pharmaceuticals(Pvt) Ltd |
Ufoxin | Trigon Pharmaceuticals Pakistan (Pvt) Ltd. |
Unifenadine | Tg Pharma |
Vasofax | Dyson Research Laboratories |
Welfast | Webros Pharmaceuticals |
Xadine | Searle Pakistan (Pvt.) Ltd. |
Xfr | Elko Organization (Pvt) Ltd. |
Xofea | Epharm Laboratories |
Xofena | Rock Pharmaceuticals |
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Adine | Pfizer Laboratories Ltd. |
Afex | Shaheen Agencies |
Aller | Lotus Pharmaceuticals (Pvt) Ltd |
Allerfedin | Heal Pharmaceuticals Pvt Ltd |
Allergofex | Leads Pharma (Pvt) Ltd |
Aloc | Bosch Pharmaceuticals (Pvt) Ltd. |
Alrin | Consolidated Chemical Laboratories (Pvt) Ltd. |
Alzera | Dr. Raza Pharma (Private) Limited |
Aspen | Zephyr Pharmatec (Pvt) Ltd. |
Axodine | Gray`S Pharmaceuticals |
Cibler | Pakistan Pharmaceutical Products (Pvt) Ltd. |
Elergifen | Semos Pharmaceuticals (Pvt) Ltd. |
Epodin | Epoch Pharmaceutical |
Exit | Fozan Pharmaceuticals Industriers (Pvt) Ltd |
Faxheal | Venture Chemical & Pharmaceuticals (Pvt) Ltd. |
Faxodine | Libra Pharmaceuticals (Pvt) Ltd |
Fekom | Karachi Chemical Industries |
Fenadex | Global Pharmaceuticals |
Fenadin | Nova Med Pharmaceuticals |
Fenadrin | Noa Hemis Pharmaceuticals |
Fendina | Highnoon Laboratories Ltd. |
Fenix | Healthtek (Pvt) Ltd |
Fenofex | Geofman Pharmaceuticals |
Fenoxy | Paramount Pharmaceuticals |
Fexet | Getz Pharma Pakistan (Pvt) Ltd. |
Fexet | Getz Pharma Pakistan (Pvt) Ltd. |
Fexigen | Genera Pharmaceuticals |
Fexinol | Martin Dow Pharmaceuticals (Pak) Ltd. |
Fexo | Hilton Pharma (Pvt) Limited |
Fexocare | Adcare Pharma |
Fexocare | Aims Pharmaceuticals |
Fexoderm | Candid Pharmaceuticals |
Fexofast | Platinum Pharmaceuticals (Pvt.) Ltd. |
Fexofax | Alliance Pharmaceuticals (Pvt) Ltd. |
Fexofin | Bio Labs (Pvt) Ltd. |
Fexokure | Kurative Pak (Pvt) Ltd |
Fexoprime | Pearl Pharmaceuticals |
Fexorex | Biorex Pharmaceuticals |
Fexosneez | Fassgen Pharmaceuticals |
Fifex | Shaigan Pharmaceuticals (Pvt) Ltd |
Fiofen | Schazoo Zaka |
Fixfast | Hygeia Pharmaceuticals |
Genfix | Genix Pharma (Pvt) Ltd |
Hasty Fort | Phar-Man Laboratories |
Histafex | Popular Chemical Works (Pvt) Ltd. |
Meadow | Macter International (Pvt) Ltd. |
Megafast | Mega Pharmaceuticals (Pvt) Ltd |
Mexodine | Mediate Pharmaceuticals (Pvt) Ltd |
Nexofen | Neo Medix |
Plexid | Atco Laboratories Limited |
Regofast | Regent Laboratories Ltd. |
Remast | Nexus Pharma (Pvt) Ltd |
Sizzle | Wilshire Laboratories (Pvt) Ltd. |
Sneez | Unimark Pharmaceuticals |
Softin-F | Welwrd Pharmaceuticals |
Tefend | Glitz Pharma |
Telfast | Sanofi Aventis (Pakistan) Ltd. |
Ufoxin | Trigon Pharmaceuticals Pakistan (Pvt) Ltd. |
Xadine | Searle Pakistan (Pvt.) Ltd. |
Xofea | Epharm Laboratories |
Xofena | Rock Pharmaceuticals |
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Telfex | Polyfine Chempharma (Pvt) Ltd. |
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Aloc | Bosch Pharmaceuticals (Pvt) Ltd. |
Axodine | Gray`S Pharmaceuticals |
Exo | English Pharmaceuticals Industries |
Faxar | Ferroza International Pharmaceuticals (Pvt) Ltd. |
Faxheal | Venture Chemical & Pharmaceuticals (Pvt) Ltd. |
Feas | Nimrall Laboratories |
Fendina | Highnoon Laboratories Ltd. |
Fendina | Highnoon Laboratories Ltd. |
Fexfa | Farm Aid Group Pak Ltd. |
Fexicame | Caraway Pharmaceuticals |
Fexinol | Martin Dow Pharmaceuticals (Pak) Ltd. |
Hifexo | Hisun Pharmaceuticals |
Kovence | Medisure Laboratories Pakistan (Pvt.) Ltd. |
Plexid | Atco Laboratories Limited |
Tefend | Glitz Pharma |
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A-Dine | Linear Pharma |
Feas | Nimrall Laboratories |
Fexicame | Caraway Pharmaceuticals |
Xyfex | Siza International (Pvt) Ltd. |