Nipa Pharmaceuticals Ltd.

  Latest
Contour Plus One meter-5%

Contour Plus One meter

 Tk.2,000.00/=  Tk.1,899.00/=
Trulicity 0.75/0.5ml

Trulicity 0.75/0.5ml

Tk.3,395.00/=
MaxD 40000 IU Capsule
Smile Baby Diaper 5's M
Smile Baby Diaper 5's S
Raja Super Condom
Amore Black Condom

Amore Black Condom

Tk.100.00/=
Amore gold condom

Amore gold condom

Tk.100.00/=
Hero Condom 1 packet
Terbin 15 gm Cream

Terbin 15 gm Cream

Tk.80.00/=
Valmor 100 Tablet

Valmor 100 Tablet

Tk.85.00/=
Tolfem 200 mg Tablet
Azaltic 15ml Susp.

Azaltic 15ml Susp.

Azaltic 15ml Susp.Description:Azaltic (Azithromycin) is an azalide antibiotic, subclass of the macrolide antibiotic, active against both Gram-positive and Gram-negative organisms. Azithromycin acts by binding to the 50S ribosomal subunit of susceptible organisms, thus interferes with the microbial protein synthesis.ndicationAzaltic (Azithromycin) is indicated for infections caused by susceptible organisms in lower respiratory tract infections including bronchitis and pneumonia, skin and soft tissue infections, otitis media and in upper respiratory tract infections including sinusitis, pharyngitis and tonsillitis. It is also indicated in the treatment of uncomplicated genital infections due to Chlamydia trachomatis & typhoid fever.Dosage & AdministrationAdult : 500 mg once daily orally for 3 days or 500 mg once on day 1, then 250 mg once on days 2-5 for 4 days. For sexually transmitted diseases caused by Chlamydia trachomatis in adults, the dose is 1 gm given as a single dose or 500 mg once on day 1, followed by 250 mg once daily for next 2 days may also be given.Children : 10 mg/kg body weight once daily for 3 days for child over 6 months or 200 mg (1 teaspoonful) for 3 days if body weight is 15-25 kg; 300 mg (1½ teaspoonfuls) for 3 days if body weight is 26-35 kg; 400 mg (2 teaspoonfuls) for 3 days if body weight is 36-45 kg. In typhoid fever, 500 mg once daily for 7-10 days is given. Azaltic (Azithromycin) should be taken at least 1 hour before or 2 hours after meal.ContraindicationAzithromycin is contraindicated in patients with known hypersensitivity to Azithromycin or any other macrolide antibiotics. Azithromycin is contraindicated in patients with hepatic diseases.PrecautionAs with any antibiotic, observation for signs of superinfection with non-susceptible organisms, including fungi, is recommended. Precaution should be taken in patients with more severe renal impairment.Side EffectsAzithromycin is well tolerated with a low incidence of side effects. The side effects include nausea, vomiting, abdominal discomfort (pain/cramps), flatulence, diarrhoea, headache, dizziness, and skin rashes which are reversible upon discontinuation of therapy.Drug InteractionAzithromycin absorption is reduced in presence of food and antacid. In patients receiving ergot alkaloids Azithromycin should be avoided because of the possibility of ergotism resulting from interaction of Azithromycin with the cytochrome P-450 system. Macrolides have been known to increase the plasma concentration of digoxin and cyclosporin. There have been no drug interactions between Azithromycin and Warfarin, Theophylline, Carbamazepine, Methylprednisolone or Cimetidine.Pregnancy & LactationPregnancy Category of Azithromycin is B. Animal reproduction studies have demonstrated that Azithromycin has no evidence of harm to the fetus. There are no adequate and well controlled studies in pregnant women. Since animal reproduction studies are not always predictive of human response, Azithromycin should be used during pregnancy only if adequate alternatives are not available. It is not known whether Azithromycin is secreted in breast milk. So, caution should be exercised when Azithromycin is administered to nursing women.Storage ConditionKeep in a dry place away from light and heat. Keep out of the reach of children...

Tk.85.00/=

  0 отзывов

Cefracef 250 Capsule

Cefracef 250 Capsule

Cefracef 250Description:Cefracef (Cefradine) is a cephalosporin antibiotic used to treat certain infections caused by bacteria such as pneumonia, nose, ear, throat, skin and urinary tract infections. It is acid stable and rapidly absorbed after oral administration. The presence of food in the gastrointestinal tract delays absorption but does not affect the total amount of Cefradine absorbed. Over 90% of this drug is excreted as unchanged in the urine within six hours.IndicationCefracef (Cefradine) is indicated in the treatment of the following infections caused by susceptible strains of the designated microorganisms: Respiratory tract infections (e.g. tonsillitis, pharyngitis and lobar pneumonia) caused by group A beta-hemolytic Streptococci and Streptococcus pneumoniae. Skin and skin structure infections caused by Staphylococci (penicillin-susceptible and penicillin-resistant) and beta-hemolytic Streptococci. Urinary tract infections including prostatitis caused by E. coli, Proteus mirabilis, Klebsiella species, and Enterococci. It is also used in otitis media caused by group A beta-hemolytic Streptococci, Streptococcus pneumoniae, Haemophilus influenzae and Staphylococci.Dosage & AdministrationAdults : For respiratory tract infections (other than lobar pneumonia) and skin and skin structure infections, the usual dose is 250 mg every 6 hours or 500 mg every 12 hours. For lobar pneumonia, the usual dose is 500 mg every 6 hours or 1 g every 12 hours.For uncomplicated urinary tract infections, the usual dose is 500 mg every 12 hours. In more serious urinary tract infections, including prostatitis, 500 mg every 6 hours or 1 g every 12 hours may be administered.Children : The usual dose in children over nine months of age is 25 to 50 mg/kg/day administered in equally divided doses every 6 or 12 hours. For otitis media due to H. influenzae, doses are from 75 to 100 mg/kg/day administered in equally divided doses every 6 or 12 hours, but should not exceed 4 g per day.ContraindicationIt is contraindicated in hypersensitivity to Cefradine or other cephalosporins.PrecautionCare is necessary with known history of allergy. Renal and hematological status should be monitored especially during prolonged and high doses therapy.Side EffectsAs with other cephalosporins, side effects are limited essentially to gastrointestinal disturbances and on occasion, to hypersensitivity phenomena, eosinophilia.Drug InteractionThe concomitant use of nephrotoxic drugs such as aminoglycosides with Cefradine may increase the risk of kidney damage. Diuretics (e.g. frusemide, ethacrynic acid) and probenecid enhanced the possibility of renal toxicity.Pregnancy & LactationUS FDA Pregnancy Category of Cefradine is B. There are, however, no adequate and well-controlled studies in pregnant women. Because animal reproduction studies are not always predictive of human response, this drug should be used during pregnancy only if clearly needed. Cefradine have been shown to be excreted in human milk. So, caution should be exercised when Cefradine is administered to a nursing woman.Storage ConditionKeep in a dry place away from light and heat. Keep out of the reach of children...

Tk.6.55/=

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Cefracef Suspension

Cefracef Suspension

CefracefDescription:Cefracef (Cefradine) is a cephalosporin antibiotic used to treat certain infections caused by bacteria such as pneumonia, nose, ear, throat, skin and urinary tract infections. It is acid stable and rapidly absorbed after oral administration. The presence of food in the gastrointestinal tract delays absorption but does not affect the total amount of Cefradine absorbed. Over 90% of this drug is excreted as unchanged in the urine within six hours.IndicationCefracef (Cefradine) is indicated in the treatment of the following infections caused by susceptible strains of the designated microorganisms: Respiratory tract infections (e.g. tonsillitis, pharyngitis and lobar pneumonia) caused by group A beta-hemolytic Streptococci and Streptococcus pneumoniae. Skin and skin structure infections caused by Staphylococci (penicillin-susceptible and penicillin-resistant) and beta-hemolytic Streptococci. Urinary tract infections including prostatitis caused by E. coli, Proteus mirabilis, Klebsiella species, and Enterococci. It is also used in otitis media caused by group A beta-hemolytic Streptococci, Streptococcus pneumoniae, Haemophilus influenzae and Staphylococci.Dosage & AdministrationAdults : For respiratory tract infections (other than lobar pneumonia) and skin and skin structure infections, the usual dose is 250 mg every 6 hours or 500 mg every 12 hours. For lobar pneumonia, the usual dose is 500 mg every 6 hours or 1 g every 12 hours.For uncomplicated urinary tract infections, the usual dose is 500 mg every 12 hours. In more serious urinary tract infections, including prostatitis, 500 mg every 6 hours or 1 g every 12 hours may be administered.Children : The usual dose in children over nine months of age is 25 to 50 mg/kg/day administered in equally divided doses every 6 or 12 hours. For otitis media due to H. influenzae, doses are from 75 to 100 mg/kg/day administered in equally divided doses every 6 or 12 hours, but should not exceed 4 g per day.ContraindicationIt is contraindicated in hypersensitivity to Cefradine or other cephalosporins.PrecautionCare is necessary with known history of allergy. Renal and hematological status should be monitored especially during prolonged and high doses therapy.Side EffectsAs with other cephalosporins, side effects are limited essentially to gastrointestinal disturbances and on occasion, to hypersensitivity phenomena, eosinophilia.Drug InteractionThe concomitant use of nephrotoxic drugs such as aminoglycosides with Cefradine may increase the risk of kidney damage. Diuretics (e.g. frusemide, ethacrynic acid) and probenecid enhanced the possibility of renal toxicity.Pregnancy & LactationUS FDA Pregnancy Category of Cefradine is B. There are, however, no adequate and well-controlled studies in pregnant women. Because animal reproduction studies are not always predictive of human response, this drug should be used during pregnancy only if clearly needed. Cefradine have been shown to be excreted in human milk. So, caution should be exercised when Cefradine is administered to a nursing woman.Storage ConditionKeep in a dry place away from light and heat. Keep out of the reach of children...

Tk.80.55/=

  0 отзывов

Diacana 100 mg Tab, 1Box

Diacana 100 mg Tab, 1Box

Diacana 100 mg Tab, 1Box..

Tk.600.00/=

  0 отзывов

Flurodent 120 ml M-WASH

Flurodent 120 ml M-WASH

Flurodent 120 ml M-WASH..

Tk.80.00/=

  0 отзывов

Nixon 1 gm IM

Nixon 1 gm IM

Nixon 1 gm IM..

Tk.220.66/=

  0 отзывов

Nixon 1 gm IV

Nixon 1 gm IV

Nixon 1 gm IV..

Tk.220.66/=

  0 отзывов

Nixon 2 gm IV

Nixon 2 gm IV

Nixon 2 gm IV..

Tk.320.96/=

  0 отзывов

Nixon 250 mg IM

Nixon 250 mg IM

Nixon 250 mg IM..

Tk.110.33/=

  0 отзывов

Nixon 250 mg IV

Nixon 250 mg IV

Nixon 250 mg IV..

Tk.110.33/=

  0 отзывов

Nixon 500 IV

Nixon 500 IV

Nixon 500 IV..

Tk.150.45/=

  0 отзывов

Nixon 500 mg IM

Nixon 500 mg IM

Nixon 500 mg IM..

Tk.150.45/=

  0 отзывов

Oxydrop 0.025% 10 ml pd nasal drops

Oxydrop 0.025% 10 ml pd nasal drops

Oxydrop 0.025% 10 ml pd nasal drops..

Tk.40.00/=

  0 отзывов

Oxydrop 0.05% 10 ml nasal drops

Oxydrop 0.05% 10 ml nasal drops

Oxydrop 0.05% 10 ml nasal drops..

Tk.45.00/=

  0 отзывов

Receca Cap 100mg, 1 Strip

Receca Cap 100mg, 1 Strip

Receca Cap 100mg, 1 Strip..

Tk.60.20/=

  0 отзывов

Esotor 40 mg Tablet (Enteric Coated), 1 strip

Esotor 40 mg Tablet (Enteric Coated), 1 strip

Esotor 40 mg Tablet (Enteric Coated), 1 stripDescription:Esotor (Esomeprazole) is a proton pump inhibitor that suppresses gastric acid secretion by specific inhibition of the H+/K+-ATPase in the gastric parietal cell. Esomeprazole (S-isomer of omeprazole) is the first single optical isomer of proton pump inhibitor, provides better acid control than racemic proton pump inhibitors.IndicationTreatment of Gastroesophageal Reflux Disease (GERD). Healing of erosive esophagitis. Maintenance of healing of erosive esophagitis. Symptomatic Gastroesophageal Reflux Disease (GERD). Reduction of NSAID-associated gastric ulcer and H. pylori eradication (Triple therapy).ContraindicationEsomeprazole is contraindicated in those patients who have known hypersensitivity to any other components of the formulation.PrecautionExclude the possibility of malignancy when gastric ulcer is suspected and before treatment for dyspepsia. When using in combination with antibiotic, refer to the prescribing information of the respective antibiotics.Side EffectsSide effects reported with Esomeprazole include headache, diarrhea and abdominal pain.Drug InteractionEsomeprazole appears to be a selective inhibitor of the cytochrome p450 mono-oxygenase system, there may be an effect on hepatic clearance, but there have been no reports to date of clinically relevant interactions. There is some uncertainty over the effect of Esomeprazole on the oral combined contraceptive pill. Physiological changes similar to those found with omeprazole are likely to take place because of the reduction in gastric acid which is likely to influence the bacterial colonization of the stomach and duodenum and also vitamin B12 absorption.Pregnancy & LactationUS FDA pregnancy category B. Studies have been performed in animals and have revealed no evidence of impaired fertility or harm to the fetus due to Esomeprazole. There are however, no adequate and well-controlled studies in pregnant women. Esomeprazole is likely to be excreted in human milk, a decision should be made whether to discontinue nursing or to discontinue the drug, taking into account the importance of the drug to the mother.Storage ConditionKeep in dry place and away from light and heat. Keep out of the reach of children...

Tk.80.20/=

  0 отзывов

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