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1 dihydroartemisinin and 40 mg piperaquine per tablet).
2 henytoin in pharmaceutical tables (100mg per tablet).
3 eutical ingredients and excipients of a drug tablet.
4 ribution in various regions of the compacted tablet.
5 ons to millimeters for the macrostrcuture of tablet.
6 thyroid range) while in therapy with L-T4 in tablet.
7 mes can be combined in a single personalised tablet.
8 healthy adults after taking a 1-mg Fluoride tablet.
9 ed in subjects with asthma treated with SLIT-tablet.
10 tion of the amorphous form of the API in the tablet.
11 eplaced by regular doses of oral misoprostol tablets.
12 e recovery towards CPZ in the pharmaceutical tablets.
13 e clinical development of timothy grass SLIT-tablets.
14 loading dose (LD) either as whole or crushed tablets.
15 o the Galaxy system through smart phones and tablets.
16 faecal discolouration) administered as oral tablets.
17 esktops, servers, laptops, smart phones, and tablets.
18 le-stranded RNA adjuvant delivered orally by tablets.
19 f reagents can be encapsulated in compressed tablets.
20 tric formulations as well as fast dissolving tablets.
21 ) for film coating of pharmaceuticals, e.g., tablets.
22 , 4.7%, and 3.8%, respectively, for caffeine tablets.
23 urine samples as well as some pharmaceutical tablets.
24 n the use of caffeinated drinks and caffeine tablets.
25 s to accelerate drug release from 3D printed tablets.
26 ect compression, producing mechanically weak tablets.
27 between the different batches of paracetamol tablets.
28 tanding of the dissolution of pharmaceutical tablets.
29 o group will receive similar-looking placebo tablets.
30 n and adults treated with timothy grass SLIT-tablets.
31 of adulterated extended-release oxymorphone tablets.
32 different assay components into color-coded tablets.
33 d by the quantification of Arg in supplement tablets.
34 er fragmentation during dissolution of these tablets.
35 acebo] to 34% [SQ house dust mite sublingual tablet]).
36 sthma were randomized to a daily SQ HDM SLIT-tablet (12 SQ-HDM dose) or placebo for up to approximate
37 thoxazole in a single fixed-dose combination tablet), 12 weeks of fluconazole, 5 days of azithromycin
38 zole prophylaxis (given as water-dispersible tablets; 120 mg per day for age <6 months, 240 mg per da
39 vir, in a once-daily, fixed-dose combination tablet (134 patients), or sofosbuvir plus weight-based r
40 ok, 2.53 [1.25]; in-person, 2.59 [1.30]; and tablet, 2.34 [1.37]) (F6,674 = 15.60; P < .001; eta2 = 0
43 e structure analysis deepen understanding of tableting across dimensions from microns to millimeters
45 d proprietary to the trial sponsor) HDM SLIT-tablet (ALK, Horsholm, Denmark) in adults and adolescent
48 ted TRAEs assessed as severe with grass SLIT-tablet and 2/60 with placebo, without a consistent trend
49 are homes, as well as local investigation of tablet and capsule impact on medication administration e
51 L161 was better tolerated than the solution; tablet and solution formulations had similar exposures,
52 hose patients currently taking many separate tablets and also allow ready tailoring of a particular d
56 s consumer electronics, such as cell phones, tablets and other portable electronic devices, are typic
57 cost interventions-low-dose oral misoprostol tablets and transcervical Foley catheterisation-are alre
58 women received routine daily iron folic acid tablets and were treated with additional iron folic acid
59 reduced to 83.1% (ACdn-EEX), 90.1% (ACdn-EEX tablet) and 93.8% (ACdn-EEX capsules) after 1 year at 5
60 tasvir (400 mg/100 mg fixed-dose combination tablet) and GS-9857 (100 mg) once daily for 6-12 weeks.
62 % (ACs-EEX), 36.0% (ACs-EES), 64.8% (ACs-EEX tablet), and 71.7% (ACs-EEX capsules) after 1 year at 5
64 material surrounding mature gastropod nacre tablets, and have only once been observed in bivalve nac
65 lacebo] to 5% [SQ house dust mite sublingual tablet]) and an increased probability of having a mild A
71 ectroscopy for the determination of water in tablets, (b) stability study in drug product development
73 ater social preference as measured using the tablet-based task was associated with increased use of s
75 via several routes: oral tablets, sublingual tablets, buccal tablets, sublingual spray, transdermal o
76 dose (achieved with similar looking placebo tablets), but not allocation up to and including week 48
77 te pressure distribution profiles within the tablet by the deformation of the crystalline particles f
81 serum TSH levels, and that switching back to tablets caused thyrotropin levels to worsen, leads us to
83 e once a day (dolutegravir group) or a three-tablet combination of ritonavir-boosted atazanavir plus
84 ect of the SQ grass sublingual immunotherapy tablet compared with placebo on the risk of developing a
85 ask to test social reward preference using a tablet computer (iPad), where two differently coloured b
86 can be transmitted to a nearby smartphone or tablet computer for post-processing, and subsequently to
89 ncer Center to report 12 common symptoms via tablet computers or to receive usual care consisting of
91 The study regimen consisted of a fixed-dose tablet containing darunavir 800 mg, cobicistat 150 mg, e
92 ssigned (2:1) to receive a once-a-day single-tablet containing elvitegravir 150 mg, cobicistat 150 mg
93 e 12 or 24 weeks of a fixed-dose combination tablet containing ledipasvir and sofosbuvir, once daily,
94 ergic rhinitis were given a daily sublingual tablet containing placebo or STG320 at a dose of 500IR,
95 or 311 days) or Group 2 (1 identical placebo tablet containing starch with no active ingredients ever
96 d 2 years of sublingual immunotherapy (daily tablets containing 15 microg of major allergen Phleum p
97 ly assigned (1:1) to receive once-daily oral tablets containing 150 mg elvitegravir, 150 mg cobicista
100 plates and can detect them from multivitamin tablets, corn flakes, energy drinks, cerebrospinal fluid
104 dings show the safety and efficacy of single-tablet darunavir, cobicistat, emtricitabine, and tenofov
106 on for up to 7 days, followed by twice-daily tablets delivering 5.5 mg/kg per day for 12 weeks).
108 ned from consecutive patients with ALS using tablet devices in waiting rooms (Knowledge Program).
109 reen-based media device (eg, cell phones and tablet devices) access or use in the sleep environment a
110 tableting technology, we show the ability of tableted diagnostics for screening hepatitis B-positive
111 asthma included in these studies, grass SLIT-tablet did not increase TEAE frequency, severe local all
112 treatment with placebo (n = 277) or HDM SLIT tablet (dosage groups: 6 SQ-HDM [n = 275] or 12 SQ-HDM [
116 d combined artemether and lumefantrine (four tablets, each containing 20 mg artemether and 120 mg lum
118 were randomly assigned to Group 1 (1 TMP-SMZ tablet every 2 days for 311 days) or Group 2 (1 identica
120 ents who were allocated eltrombopag received tablets (except for those aged 1-5 years who received an
121 ion plus once-daily dapagliflozin 10 mg oral tablets, exenatide with dapagliflozin-matched oral place
122 harmacokinetics, and efficacy of this single-tablet, fixed-dose combination of elvitegravir, cobicist
124 dardised quality) house dust mite sublingual tablet for 1 year resulted in a decreased probability of
126 first North American trial of use of a SLIT-tablet for HDM allergy, 12 SQ-HDM was well tolerated and
127 65-year-old female whom took lactate calcium tablets for 5 years presented with progressive dysphagia
128 of coffee, caffeinated drinks, and caffeine tablets for CE and potential factors derived from profes
130 ment strategies of iodine supplementation in tablet form with no iodine supplementation for pregnant
131 al gefitinib 250 mg or placebo once daily in tablet form; randomisation did not include stratificatio
132 s an opioid antagonist which as a once-a-day tablet formulation has recently been approved for reduci
143 SQ house dust mite sublingual immunotherapy tablets has been demonstrated in patients with allergic
147 The map of deformation degrees within the tablet illustrated the heterogeneous pressure distributi
148 d the efficacy and safety of the SQ HDM SLIT-tablet in adults with moderate-to-severe HDM-induced all
149 Using data from eight trials of grass SLIT-tablet in subjects with allergic rhinitis with/without c
151 grass pollen sublingual immunotherapy (SLIT) tablets in AR and their impact on asthma onset and progr
152 al to assess the efficacy/safety of HDM SLIT-tablets in North American subjects with HDM-induced alle
154 e efficacy of these sublingual immunotherapy tablets in the treatment of allergic rhinitis has been f
156 assess the safety and efficacy of the single tablet integrase inhibitor regimen containing elvitegrav
160 exhibit complete brittle fracture along the tablet interfaces at the proportional limit under pure s
161 DM) sublingual allergen immunotherapy (SLIT) tablet is a potential novel treatment option for HDM all
162 tial resolution to resolve microparticles in tablets is essential to ensure high quality and efficacy
164 g 2000 UA/day monomeric allergoid sublingual tablets is well tolerated and reduces the CPT reaction i
166 l activity of these clinically effective TIM tablets led in the same range (6200-8200 BAU; 0.92-1.23
169 were switched back again to receive L-T4 in tablets, maintaining the dosage, TSH levels worsened aga
170 controlled, phase 3 trial evaluated olaparib tablet maintenance treatment in platinum-sensitive, rela
173 ady-to-use inactivated yeast interfering RNA tablets may one day facilitate the seamless integration
175 cebo-controlled trials of Timothy grass SLIT-tablet MK-7243 (2800 BAU/75 000 SQ-T, Merck/ALK-Abello)
176 f action of the HDM sublingual immunotherapy tablet MK-8237 (Merck/ALK-Abello) using the Vienna Chall
177 t mite (HDM) sublingual immunotherapy (SLIT) tablet (MK-8237; Merck & Co, Kenilworth, NJ/ALK-Abello,
179 D3 (2400 IU/d; n = 315) or matching placebo tablets (n = 308) from pregnancy week 24 to 1 week postp
180 (VACV) 2 g thrice daily (n = 40) or placebo tablets (n = 47) for 90 days (12 tablets of study medica
181 1.19]; in-person [n = 165], 2.66 [1.11]; and tablet [n = 71], 2.53 [1.17]) and at 12 months (workbook
183 ents aged 12-17 years received a combination tablet of 90 mg ledipasvir and 400 mg sofosbuvir once da
184 Patients were given a fixed-dose combination tablet of 90 mg ledipasvir and 400 mg sofosbuvir orally
185 perienced) received a fixed-dose combination tablet of 90 mg of ledipasvir and 400 mg of sofosbuvir o
188 patients received the fixed-dose combination tablet of LDV-SOF once-daily plus weight-based RBV (1,00
189 igned to groups given fixed-dose combination tablet of ledipasvir and sofosbuvir (n = 25) or ledipasv
190 The first received a fixed-dose combination tablet of ledipasvir-sofosbuvir (90/400 mg) once daily f
191 t with the once-daily fixed-dose combination tablet of ledipasvir/sofosbuvir (LDV/SOF) with and witho
193 eive treatment with a fixed-dose combination tablet of sofosbuvir-velpatasvir-voxilaprevir with or wi
195 ollowed by once daily combination fixed-dose tablets of 90 mg ledipasvir and 400 mg sofosbuvir plus w
199 of treatment with 500IR and 300IR sublingual tablets of HDM allergen extracts was efficacious and wel
202 They were randomized to receive either 60 tablets of placebo; cyclobenzaprine, 5 mg; or oxycodone,
204 in which participants were given combination tablets of tenofovir disoproxil fumarate (300 mg) and em
208 ed solid, orally administered medications in tablet or capsule form at ten purposively sampled care h
210 ate the phytochemical content in 10 samples (tablets or capsules), showing concentrations of (+)-cate
211 articipants received oral cabotegravir 30 mg tablets or matching placebo once daily during a 4 week o
213 :1) to receive either eltrombopag or placebo tablets (or oral suspension formulation if aged 1-5 year
214 nts received sublingual immunotherapy (SLIT) tablet (Oralair, Stallergenes(c)) and symptomatic therap
215 orally once daily or raltegravir 400 mg (one tablet) orally twice daily, each with tenofovir disoprox
216 se system to raltegravir 1200 mg (two 600 mg tablets) orally once daily or raltegravir 400 mg (one ta
217 cacy and safety of 2 doses of HDM sublingual tablets over 1 treatment year and the subsequent immunot
219 families, 23 expressed a preference for the tablet PC over the notebook, 3 had no preference, and 4
225 use of at least 0.5 to 1.5 standard aspirin tablets per week; the minimum duration of regular use as
234 t with the SQ grass sublingual immunotherapy tablet reduced the risk of experiencing asthma symptoms
235 han 50% of the expected number of vismodegib tablets; reduction in the number of surgical excisions r
236 y, and tolerability of switching to a single-tablet regimen containing rilpivirine, emtricitabine, an
237 isoproxil fumarate (TDF) as a 3-drug, single-tablet regimen for PEP in men who have sex with men (MSM
239 efficacy and safety of switching to a single-tablet regimen of darunavir, cobicistat, emtricitabine,
240 ly assigned (1:1) to receive either a single-tablet regimen of dolutegravir plus abacavir and lamivud
241 alafenamide (25 mg) or to continue a single-tablet regimen of efavirenz (600 mg), emtricitabine (200
242 randomly assigned (1:1) to receive a single-tablet regimen of either rilpivirine (25 mg), emtricitab
244 randomly assigned (1:1) to receive a single-tablet regimen of rilpivirine (25 mg), emtricitabine (20
245 alafenamide (25 mg) or to remain on a single-tablet regimen of rilpivirine (25 mg), emtricitabine (20
248 usehold water storage container, the ceramic tablet releases silver ions at a controlled rate that in
249 patients and investigate IV exposure to the tablet's inert ingredients as a possible causal mechanis
252 ay diffractograms of the powders and crushed tablets show evidence of the formation of new crystallin
254 t with the SQ grass sublingual immunotherapy tablet significantly reduced the risk of experiencing as
256 e events (AEs) with sublingual immunotherapy tablet (SLIT-tablet) treatment, such as severe systemic
258 es: oral tablets, sublingual tablets, buccal tablets, sublingual spray, transdermal ointment, and tra
259 ations for delivery via several routes: oral tablets, sublingual tablets, buccal tablets, sublingual
261 to follow crystallization of indomethacin on tablet surfaces under two storage conditions: 30 degrees
264 In seasonal allergy trials with grass SLIT-tablet, the observed treatment effect is highly dependen
266 mine the biological activity of solution and tablet Timothy grass pollen (TIM) extracts, compared to
269 ) with sublingual immunotherapy tablet (SLIT-tablet) treatment, such as severe systemic reactions and
271 ntire pollen seasons in 6 timothy grass SLIT-tablet trials (n = 3094) and 2 ragweed SLIT-tablet trial
272 -tablet trials (n = 3094) and 2 ragweed SLIT-tablet trials (n = 658) and during the last 8 weeks of t
274 eneity and use of rescue medications in SLIT-tablet trials, effects on nasal symptoms with timothy gr
278 were randomly assigned to simvastatin 20 mg tablets twice-daily plus vitamin D3 1,000 international
279 ive extended-pulsed fidaxomicin (200 mg oral tablets, twice daily on days 1-5, then once daily on alt
280 signed 2:1 to olaparib (300 mg in two 150 mg tablets, twice daily) or matching placebo tablets using
281 mg tablets, twice daily) or matching placebo tablets using an interactive voice and web response syst
282 hes of analgesic paracetamol (acetaminophen) tablets using nitrogen-14 nuclear quadrupole resonance s
283 ess the safety and immunogenicity of an oral tablet vaccine against influenza A H1N1 in healthy adult
284 children with asthma treated with grass SLIT-tablet versus subjects without asthma in or outside of p
285 atment of AR patients with grass pollen SLIT tablets was associated with slower AR progression, less
286 The treatment effect of timothy grass SLIT-tablets was considered similar between pediatric (n = 79
287 icacy of rBet v 1 formulated as a sublingual tablet were assessed in a multicentre, double-blind, pla
288 , AR patients treated with grass pollen SLIT tablets were compared with a control group not having re
290 symptoms with timothy grass and ragweed SLIT-tablets were nearly as great as with MFNS and numericall
297 or triple fixed-dose-combination paediatric tablets with lamivudine and nevirapine or efavirenz.
298 nt effect of sublingual immunotherapy (SLIT)-tablets with pharmacotherapy for seasonal allergic rhini
299 s receiving once daily for 5 months rBet v 1 tablets, with a mean difference of 17.0-17.7% relative t
300 o investigate the effects of Xueshuan Xinmai tablets (XXMT) on neurologic deficits, quality of life a
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