What are the interactions of Duolin Inhaler ? The Inhaler is used for the treatment and prevention from conditions and symptoms of diseases like asthma, respiratory disease, lung disorder, nasal cavity blockage and inflammation of the mucous membrane. Duolin Respules 2.5Ml is used for Chronic Obstructive Pulmonary Disorder (Copd) etc. 2002
500 mg PO q8hr for 7 days; initiated within 72 hours of symptom or lesion onsetTreatment of initial and recurrent episodes or suppressive therapy in immunocompetent adultsRecurrent episodes: 1500 mg PO once; initiate therapy at first sign (within 1 hour) of symptoms such as tingling, itching or burningTreatment of initial and recurrent episodes or suppressive therapy in immunocompetent adultsInitial episode (off-label): 250 mg PO q8hr for 7-10 daysSuppressive therapy: 250 mg PO q12hr for up to 12 monthsRecurrent episodes: 1000 mg PO q12hr for 1 day; initiated within 6 hours of symptom or lesion onsetPrevention of herpes simplex virus (HSV) reactivation and treatment of recurrent episodesRecurrent episodes: 500 mg PO q12hr for 5-10 days; initiated within 48 hours of symptom or lesion onsetTreatment of initial and recurrent episodes or suppressive therapy<18 years: Safety and efficacy not established; may be considered in adolescentsSuppressive therapy: 250 mg PO q12hr for up to 12 monthsRenal impairment: As for adults; see Dosing ModificationsBlood and lymphatic system disorders: ThrombocytopeniaImmune system disorders anaphylactic shock and anaphylactic reaction underHepatobiliary disorders: Abnormal liver function tests, cholestatic jaundiceNervous system disorders: Dizziness, somnolence, seizuresPsychiatric disorders: Confusion (including delirium, disorientation, and confusional state occurring predominantly in the elderly), hallucinationsSkin and subcutaneous tissue disorders: Urticaria, Stevens-Johnson syndrome, toxic epidermal necrolysis, angioedema (eg, face, eyelid, periorbital, pharyngeal edema), hypersensitivity vasculitisKnown hypersensitivity to this drug or its active metabolite, penciclovirDosage must be adjusted in renal impairment; there is a risk of acute renal failure (ARF) with inappropriately high dosagePatients with galactose intolerance, glucose-galactose malabsorption syndrome, or severe lactase deficiency should discuss it with practitioner (famciclovir tablets contain lactose)Healthcare providers are encouraged to report pregnancies and pregnancy outcomes to Novartis Adverse Event reporting line at 1-888-NOW-NOVA (669-6682)Available data from pharmacovigilance reports in pregnant women have not identified a drug- associated risk of major birth defects, miscarriage or adverse maternal or fetal outcomes; there are risks to fetus associated with untreated herpes simplex virus during pregnancy; after oral administration, famciclovir (prodrug) is converted to penciclovir (active drug); in animal reproduction studies with famciclovir, no evidence of adverse developmental outcomes observed at systemic exposures of penciclovir (AUC) slightly higher than those at maximum recommended human dose (MRHD)The risk of neonatal herpes infection varies from 30% to 50% for genital herpes simplex virus (HSV) infections that occur in late pregnancy (third trimester), whereas in early pregnancy, infection carries a risk of about 1%; primary herpes outbreak during first trimester of pregnancy associated with neonatal chorioretinitis, microcephaly and, in rare cases, skin lesions; in very rare cases, transplacental transmission can occur resulting in congenital infection, including microcephaly, hepatosplenomegaly, intrauterine growth restriction and stillbirth; co-infection with HSV increases the risk of perinatal HIV transmission in women who had a clinical diagnosis of genital herpes during pregnancyThere are no data on presence of famciclovir (prodrug) or penciclovir (active drug) in human milk, effects on breastfed infant, or on milk production; animal data indicate that penciclovir is present in the milk of lactating rats; developmental and health benefits of breastfeeding should be considered along with mother’s clinical need for therapy and any potential adverse effects on breastfed infant from therapy or from underlying maternal conditionA: Generally acceptable. Plus she need to take oral tablets for 15-20 days. This medication is a short acting adrenergic receptor. Diseases & Conditions
Asthma is a chronic lung condition wherein the air passage gets blocked or constricted due to the production of extra mucus.
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