and dispense with the product.IF YOU NEED TO USE YOUR INHALER BEFORE IT IS Plasma levels of albuterol sulfate and HFA-134a after inhaled therapeutic doses are very low in humans, but it is not known whether the components of PROVENTIL HFA Inhalation Aerosol are excreted in human milk. about submitting notices and www.HIPAASpace.com policy about responding to notices in our Help Center. The expected symptoms with overdosage are those of excessive beta-adrenergic stimulation and/or occurrence or exaggeration of any of the symptoms listed under including cleft palate and limb defects, have been reported in the offspring of with PROVENTIL HFA Inhalation Aerosol, compared to other albuterol inhalation PROVENTIL HFA Inhalation Aerosol should be discarded when the dose indicator display window shows zero. For best results, canister should be at room temperature before use.The yellow actuator supplied with PROVENTIL HFA Inhalation Aerosol should not be used with any other product canisters, and actuator from other products should not be used with a PROVENTIL HFA Inhalation Aerosol canister. It is recommended Each actuation of circulation to the fetus.There are no adequate and well-controlled studies of PROVENTIL HFA Inhalation study in CD-1 mice given albuterol sulfate subcutaneously showed cleft palate Due to inconsistencies between the drug labels on DailyMed and the pill images provided by In some patients, one inhalation every 4 hours may be sufficient. bronchospasm as demonstrated by the maintenance of FEVIn a 4-week, randomized, open-label trial, 63 children, 4 to 11 years of age, As with all sympathomimetic medications, cardiac arrest and even death may be associated with abuse of PROVENTIL® HFA Inhalation Aerosol. A study in which pregnant rats were dosed with radiolabeled albuterol sulfate demonstrated that drug-related material is transferred from the maternal circulation to the fetus.

the patient's physician.4. Rx only.

NDC Code(s): 0085-1132-04 Packager: Merck Sharp & Dohme Corp. PROVENTIL HFA (albuterol sulfate) aerosol, metered. Each actuation delivers 120 mcg of albuterol sulfate from the valve and 108 mcg of albuterol sulfate from the mouthpiece (equivalent to 90 mcg of albuterol base).

the incidence of all adverse events (whether considered by the investigator drug Proventil HFA inhalation aerosol, Merck, 0.09 mg/1 actuation, 6.7 gram metered dose inhaler, 1 count, NDC 00085-1132-04; Ventolin HFA inhalation aerosol, GlaxoSmithKline, 0.09 mg/1 actuation, 18 gram metered dose inhaler, 1 count, NDC 00173-0682-20 Store between 15°-25°C (59°-77°F). NDC Code(s): 50090-4326-0, 50090-4326-1 Packager: A-S Medication Solutions; This … It is recommended to prime the inhaler before using for the first time and in cases where the inhaler has not been used for more than 2 weeks by releasing four “test sprays” into the air, away from the face. NDC 0085-1132-04. concurrently. By using our Services, you agree that www.HIPAASpace.com can use such data Remove the inhaler from your mouth, and then breathe out.It is very important that you keep the mouthpiece clean so that medicine will not build up and block the spray through the mouthpiece. Time to maximum plasma concentration (Tmax) and mean residence time are both extremely short, leading to a transient appearance of HFA-134a in the blood with no evidence of accumulation. A The molecular weight of albuterol sulfate is 576.7, and the empirical formula is (C mesovarium at the above dietary doses of 2 mg/kg (approximately 15 times the The dose indicator display will move after every tenth actuation. asthmatic symptoms, the usual dosage for adults and children 4 years of age and 54868-6051-0 All rights reserved. Effective and safe use of PROVENTIL HFA Inhalation Aerosol includes an understanding of the way that it should be administered. There is insufficient evidence to determine if dialysis is beneficial for overdosage of PROVENTIL HFA Inhalation Aerosol. isoproterenol at comparable doses while producing fewer cardiovascular effects. recommended. 0085-1132-02 Exposure to temperatures above 120°F may cause bursting. The safety and effectiveness of PROVENTIL HFA Inhalation Aerosol in pediatric patients below the age of 4 years have not been established. symptoms listed under Hypokalemia may also occur. (CEach actuation delivers 120 mcg albuteraol sulfate, USP from the valve and