Monounsaturated Fatty Acid diet associates less gastrointestinal adverse events of pirfenidone: phase IV clinical trial

Author(s):  
Eva Fontanilles ◽  
Carlo Vancheri ◽  
Marlies Wijsenbeek ◽  
Katerina Antoniou ◽  
Pilar Rivera ◽  
...  
2018 ◽  
Vol 5 (6) ◽  
Author(s):  
H Keipp Talbot ◽  
Andrew J Dunning ◽  
Corwin A Robertson ◽  
Victoria A Landolfi ◽  
David P Greenberg ◽  
...  

Abstract Passive surveillance data had signaled the possibility of gastrointestinal adverse events occurring after the administration of high-dose inactivated influenza vaccine (IIV-HD). However, in a large, prospective randomized clinical trial, rates of serious gastrointestinal events were no greater among IIV-HD recipients than among those who received a standard-dose influenza vaccine.


Author(s):  
JoséL. Periago ◽  
Carolina De Lucchi ◽  
Angel Gil ◽  
M.Dolores Suárez ◽  
Maria L. Pita

2006 ◽  
Vol 7 (3) ◽  
pp. 443
Author(s):  
S. Desroches ◽  
A. Tchernof ◽  
W.R. Archer ◽  
P. Couture ◽  
N. Bergeron ◽  
...  

1991 ◽  
Vol 180 (1) ◽  
pp. 162-168 ◽  
Author(s):  
Jesus Osada ◽  
Antonio Fernandez-Sanchez ◽  
Jose Luis Diaz-Morillo ◽  
Hortensia Aylagas ◽  
Maria Jesus Miro-Obradors ◽  
...  

Author(s):  
Dr. Mayuresh Dilip Kiran ◽  
Lalit Jeevan Pawaskar ◽  
Shaheen Naseem Sheikh

Background: Cough is one of the most common symptom that most of the Doctors faces while practising in paediatric population. Cough can be productive or unproductive. Productive cough can be treated with the combination of bronchodilator, expectorant and mucolytics. The main objective of the Phase IV clinical trial conducted was to test the efficacy and safety for the combination of Levosalbutamol (bronchodilator), Ambroxol Hydrochloride (mucolytic agent) and Guaifenesin (expectorant) for the treatment of productive cough associated with bronchospasm in conditions such as bronchitis and bronchial asthma as well as all conditions associated with tenacious mucus, wheezing and chest congestion. Methodology: The trial was conducted with 23 paediatric speciality Doctors on 325 patients out of which 149 patients were of age group 2 to 12 years and 176 were of age below 1 year. Efficacy assessment was done by analysing the cough severity score at all the visits. Safety assessment was done by analysing the adverse events experienced by the patients or observed by the investigators at all the visits. Results: At baseline, CSS was 6.624 reduced to 3.744 at day 3 and 1.049 at day 5. One point reduction in Likert type symptom scale from moderate to mild was in just 5 days. Only 12.923 % of patients experienced non-serious adverse events. Conclusion: Combination of Levosalbutamol, Ambroxol Hydrochloride and Guaifenesin was safe as well as efficacious for the treatment of productive cough.


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