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10,216 Possible Causes for 12, Capsule, Dose, Form, Hours, Release, Sustained

  • Carbidopa-Levodopa

    During 12-h clinic visits on day 10, plasma samples were collected for pharmacokinetics, and motor performance was assessed hourly.[] […] examined the effects of supplemental standard carbidopa/levodopa (Std-L) on early morning akinesia in patients with Parkinson's disease (PD) who were being treated with sustained-release[] Code & Prescriber Medicinal Product Pack (Name, form & strength and pack size) Max qty packs Max qty units No. of repeats DPMQ Max Safety Net General Patient Charge 1242J[] LD concentrations from ER CD---LD were sustained for approximately 5 hours and did not decrease to 10% of peak until 10.1 hours.[] A new extended-release (ER) carbidopa-levodopa capsule product (also referred to as IPX066) was developed and approved in the US as Rytary and in the EU as Numient .[] In this single-dose study, there were no significant differences in pharmacokinetic and motor responses between Sinemet and Atamet.[] We aimed to assess this extended-release formulation versus immediate-release carbidopa-levodopa in patients with Parkinson's disease and motor fluctuations.[]

  • Phendimetrazine

    11 12 1 13 7 12 1 14 9 13 1 15 8 14 1 #Up[] Abstract Two tablet formulations of d-phendimetrazine bitartrate, Obex (35 mg non-sustained action) and Obex-LA (105 my sustained action), were compared in terms of biological[] Bontril Slow-Release capsules contain FD&C Yellow No. 6 as a color additive.[] Phendimetrazine Dosing: An Introduction The dose of phendimetrazine tartrate ( Bontril ) that your healthcare provider prescribes will vary, depending on a number of factors[] Elite Pharmaceuticals, Inc. develops oral sustained and controlled release products.[] […] oral phendimetrazine (35, 70, and 105 mg), d-amphetamine (10, 20, and 30 mg), and placebo were assessed in quasi-random order across 8 sessions lasting for approximately 8 hours[] PO- 1 tablet (35 mg) 2 or 3 times/day, one hour before meals.[]

  • Nifedipine

    METHODS: AdADOSE was a 12-week, international, multicenter, prospective, observational study.[] The authors present a case of a 25-year-old previously healthy woman with massive overdose of sustained-release nifedipine resulting in severe hypotension.[] […] of the active pharmaceutical ingredient (API) nifedipine are reviewed to evaluate whether a waiver of in vivo bioequivalence (BE) testing of immediate-release (IR) dosage forms[] 48 hours, and 1 week after tocolytic treatment.[] Abstract Over the past 2 decades, nifedipine in the form of capsules has become widely popular in the treatment of hypertensive emergencies.[] CONCLUSION: A low-dose combination of nifedipine GITS plus valsartan or high-dose nifedipine was more effective in improving central hemodynamics than high-dose valsartan[] Abstract Nifedipine immediate release (IR) is a short-acting dihydropyridine calcium channel blocker historically used for hypertensive crisis, but its use has decreased because[]

  • Hydromorphone

    12.[] Buprenorphine, a μ-opioid receptor partial agonist and kappa opioid receptor antagonist, is now being developed as a monthly, sustained-release formulation (RBP-6000).[] Code & Prescriber Medicinal Product Pack (Name, form & strength and pack size) Max qty packs Max qty units No. of repeats DPMQ Max Safety Net General Patient Charge 5115F[] His lawyers filed an appeal for an emergency stay of execution, after he had been "gasping and snorting for more than an hour" in the death chamber.[] Data Summary A pharmacokinetic study in healthy subjects showed that co-ingestion of a 12-mg Palladone capsule with 240 mL (8 ounces) of 40% (80 proof) alcohol resulted in[] On hospital day 1, intravenous hydromorphone (6 doses, total dose of 4 mg) was administered.[] Dose selection of a once-daily, osmotic-controlled extended-release (ER) hydromorphone assumes that this drug and immediate-release (IR) hydromorphone are dose equivalent.[]

  • Tolterodine

    METHODS: From January 2007 to December 2008, 250 patients with a Qmax less than 12 ml/s were selected for this study.[] Therefore, the developed sustained-release tablet formulation of TOL could be an alternative dosage form to the SR capsule for treatment of OAB.[] METHODS: The effect of three microemulsions formed by Labrasol: Plurol (3:1), isopropyl myristate and water on the permeation of tolterodine through miniature pig skin was[] […] found at 12.00-18.00, 18.00-24.00, and 24.00-06.00 hours with a between-group difference at 18.00-24.00 hours (coefficient 542 mL, P 0.01).[] The capsules are marked with MYLAN over 3402 in black ink on both parts of the capsule.[] OBJECTIVE: The purpose of this study was to develop hydroxypropylmethylcellulose (HPMC)-based sustained release (SR) tablets for tolterodine tartrate with a low drug release[] We observed much stronger induction of ABCB1 mRNA by S-tamsulosin as compared to the R or racemic form.[]

  • Dextroamphetamine

    The current study was a double-blind, placebo-controlled, study in which volunteers received either 1000 mg sodium valproate (n 12), 900 mg lithium (n 9), or placebo (n 12[] Stimulants are easy to use and popular for sustaining performance because their utility is not dependent upon environmental or scheduling modifications.[] Two major polymorphic forms of human FMO3 were studied, and the results suggested preferential N-oxygenation by only one of the two enzymes.[] Systolic blood pressures of males were elevated from 1 hour after the first 10-mg dose until 5 hours after the third 10-mg dose.[] , EXTENDED RELEASE in 1 BOTTLE CII 52054-513 HUMAN PRESCRIPTION DRUG DEXEDRINE (SPANSULE) dextroamphetamine sulfate CAPSULE, EXTENDED RELEASE ORAL 08-02-1976 NDA NDA017078[] The subjects took 60 mg sustained-release d-AMP for 8 weeks, during which time they received eight 50-min sessions of individual psychotherapy.[] METHODS: This was a double-blind, placebo-controlled, study in which volunteers received either 1000 mg sodium valproate (n 12), 900 mg lithium (n 9) or placebo (n 12).[]

  • Diltiazem

    The present work reports the evaluation of three nonionic ether-monohydroxyl surfactants (C(12)E(1), C(12)E(5,) and C(12)E(8)) as skin permeation enhancers in the transdermal[] The patient presented within 3 h following acute ingestion of multiple medications including sustained-release diltiazem.[] The Mylan is a SR diffusion coated beads form whereas the IntelliCap is a monolithic capsule.[] […] tabletCardizem LA 360 mg 24 Hour tablet4.81USD tabletCardizem LA 300 mg 24 Hour tablet4.71USD tabletDiltiazem HCl Coated Beads 360 mg 24 Hour tablet4.62USD tabletCardizem[] Cardizem CD capsules are available online form Inhouse Pharmacy in 3 doses: 120mg CDcapsule 180mg CD capsules 240mg CD capsules Treating hypertension (high blood pressure)[] Adult patients were categorized by the dose of diltiazem received; 10 mg standard dose or 0.2-0.3 mg/kg WB dose.[] However, no studies exist comparing oral (PO) immediate release and IV continuous infusion diltiazem in the emergency setting.[]

  • Oxycodone

    He told her to take OxyContin every 12 hours.[] RESULTS: Plasma profiles of OOD reveal sustained concentrations of oxycodone over the complete dosing interval of 24 hours.[] Is this a new form of non-Ig-associated fibrillary glomerulopathy with its pathogenesis linked to some component of the oxycodone suppositories?[] Oxycodone extended release capsules are an extended-release (ER), microsphere-in-capsule abuse-deterrent-formulation designed to retain its extended-release properties following[] A case report of a cancer patient who was receiving increasing doses of oxycodone with an unexpected declining analgesia is presented.[] Controlled-release oxycodone is absorbed in a bi-exponential fashion.[] It is most commonly available in prescription form as either OxyContin or Percocet. OxyContin is a popular painkiller that is intended for slow release over 12 hours.[]

  • Sunburn

    Apply yogurt Yogurt with live cultures can also be applied on the affected skin. 12. Apply cold water or ice Water is virtually everywhere. Use it to soothe burnt skin.[] There has been a sustained decrease in weekend sunburn among adolescents and adults.[] Overall, based on the studies, there is evidence that polyphenols in both oral and topical form may provide protection from UV damage and sunburn, and thus are beneficial[] If you want to know how to heal a sunburn in just under 24 hours, I’ve got a trick for you. All it takes is two simple, real foods.[] Break open a capsule and apply the vitamin directly to your burn to encourage the healing process.[] High personal UVR doses can be gained during leisure activities, causing intense self-resolving inflammation (sunburn) of unprotected skin.[] Ultraviolet (UV) B-induced hydrolysis of membrane phospholipids releases polyunsaturated fatty acids, and their subsequent metabolism by cyclooxygenases (COXs) and lipoxygenases[]

  • Theophylline

    Pain intensity was assessed 2, 6, and 12 hour after drug administration using 0-10 cm Visual Analog Scale.[] Subsequent to this, sustained low-efficiency dialysis (SLED) was undertaken.[] Article First Online: 24 June 2009 830 Downloads 17 Citations Abstract The physicochemical properties of theophylline hydrate and anhydrous polymorphic forms I and II were[] GENERIC NAME: THEOPHYLLINE - ORAL 24 HOUR TABLET (thee-OFF-ih-lin) BRAND NAME(S): Uni-Dur Medication Uses How To Use Side Effects Precautions Drug Interactions Overdose Notes[] capsules (Identified UM) 10 mg orange capsules (Identified UM) Storage And Handling MARINOL (dronabinol capsules, USP) 2.5 mg white capsules (Identified UM).[] At therapeutic dose, an alteration of theophylline metabolism had happened, that induced a decrease on the theophylline clearance coinciding with an increase of dose.[] […] as a potential candidate for the release of theophylline.[]