A Safety Study of Balsamic Bactrim in Pediatric Participants With Acute Bronchitis
- Respiratory Disorder
The source of the below information is public registry websites such as ClinicalTrials.gov, EuClinicalTrials.eu, ISRCTN.com, etc.. It has been summarised and edited into simpler language. For more information about this clinical trial see the For Expert tab on the specific ForPatients page or follow these links to https://clinicaltrials.gov and/or https://euclinicaltrials.eu and/or https://www.isrctn.com.
The below information is taken directly from public registry websites such as ClinicalTrials.gov, EuClinicalTrials.eu, ISRCTN.com, etc., and has not been edited.
This pilot, multicentric and observational study will assess the safety of sulfamethoxazole + trimethoprim + guaifenesin (Balsamic Bactrim) in pediatric participants with acute bronchitis. Administration of treatment will be according to treating physician's recommendation under local labeling.
A Pilot, Multicentric and Observational Study of Safety of Sulfamethoxazole + Trimethoprim + Guaifenesin (Balsamic Bactrim) in Pediatric Patients With Acute Bronchitis
- Participants starting treatment with Bactrim Balsamic suspension
- Participants with a clinical diagnosis of acute bronchitis (cough with or without sputum production less than 30 days) according to the medical criteria
- Participants who have started treatment with another antibiotic at the time of the visit
- Participants with no respiratory infections
- Participants with mental disorders that do not permit the clinical evaluation of the participant according to the treating physician's criteria
- Participants with severe hepatic parenchymal damage
- Participants with severe renal failure making it difficult to monitor drug plasma concentration
- Participants with hypersensitivity to any of Balsamic Bactrim active ingredients, excipients, and/or sulfas
For the latest version of this information please go to www.forpatients.roche.com