Pseudoephedrine sulphate: Its elimination half-life in humans, at an approximate urinary pH of 6, ranges from 5 to 8 hours. The active substance and its metabolite are excreted in urine; 55-75 % of the administered dose is excreted unchanged.

Having regard to the particular characteristics of these homeopathic medicinal products, such as the very low level of active principles they contain and the difficulty of applying to them the conventional statistical methods relating to clinical trials, it is desirable to provide a special, simplified registration procedure for those homeopathic medicinal products which are placed on the market without therapeutic indications in a pharmaceutical form and dosage which do not present a risk for the patient.

In a single trial, where gemcitabine at a dose of 1,000 mg/m2 was administered concurrently for up to 6 consecutive weeks with therapeutic thoracic radiation to patients with non-small cell lung cancer, significant toxicity in the form of severe, and potentially life threatening mucositis, especially oesophagitis, and pneumonitis was observed, particularly in patients receiving large volumes of radiotherapy [median treatment volumes 4,795 cm3].

These medicines are not recommended with Telzir/ ritonavir: • doses of ketoconazole and itraconazole greater than 200 mg per day (used to treat fungal infections) • doses of rifabutin greater than 150 mg every other day (an antibiotic) • lidocaine given by injection (an anaesthetic) • halofantrine (used to treat malaria) • midazolam and triazolam (used to treat anxiety) • sildenafil and vardenafil (used to treat erectile dysfunction) • lovastatin, simvastatin and doses of atorvastatin greater than 20 mg per day (used to lower cholesterol) • fluticasone propionate and similar medicines used to treat asthma, unless considered essential.

62 • doses of ketoconazole and itraconazole greater than 200 mg per day (used to treat fungal infections) • doses of rifabutin greater than 150 mg every other day (an antibiotic) • lidocaine given by injection (an anaesthetic) • halofantrine (used to treat malaria) • midazolam and triazolam (used to treat anxiety) • sildenafil and vardenafil (used to treat erectile dysfunction) • lovastatin, simvastatin and doses of atorvastatin greater than 20 mg per day (used to lower cholesterol) • fluticasone propionate and similar medicines used to treat asthma, unless considered essential.

In the European Union (EU), Moxifloxacin film coated tablet are indicated for the treatment of acute bacterial sinusitis (ABS), acute exacerbation of chronic bronchitis (AECB) and community acquired pneumonia (CAP) except severe cases, at the dose of 400 mg daily for 7 days for ABS, 5-10 days for AECB and for 10 days for CAP.

In a subsequent randomised open-label study (ESS100732) in antiretroviral naïve patients, fosamprenavir (700 mg) co-administered with low dose ritonavir (100 mg) in a twice daily regimen including abacavir / lamivudine (600 mg / 300 mg) fixed dose combination tablet once daily showed comparable efficacy over 48 weeks to lopinavir / ritonavir (400 mg / 100 mg) given twice daily in combination with abacavir / lamivudine (600 mg / 300 mg once daily).

• Lithium containing medicines to treat some types of depression. • Medicines that may increase blood potassium levels such as salt substitutes containing potassium, potassium-sparing diuretics (certain 'water tablets '), ACE inhibitors, angiotensin II receptor antagonists, NSAIDs (non steroidal anti-inflammatory medicines, e. g. aspirin or ibuprofen), heparin, immunosuppressives (e. g. cyclosporin or tacrolimus), and the antibiotic trimethoprim. • Diuretics ('water tablets '), especially if taken in high doses together with Pritor, may lead to excessive loss of body water and low blood pressure (hypotension).

• Lithium containing medicines to treat some types of depression. • Medicines that may increase blood potassium levels such as salt substitutes containing potassium, potassium-sparing diuretics (certain 'water tablets '), ACE inhibitors, angiotensin II receptor antagonists, NSAIDs (non steroidal anti-inflammatory medicines, e. g. aspirin or ibuprofen), heparin, immunosuppressives (e. g. cyclosporin or tacrolimus), and the antibiotic trimethoprim. • Diuretics ('water tablets '), especially if taken in high doses together with Micardis, may lead to excessive loss of body water and low blood pressure (hypotension).

• Lithium containing medicines to treat some types of depression. • Medicines that may increase blood potassium levels such as salt substitutes containing potassium, potassium-sparing diuretics (certain 'water tablets '), ACE inhibitors, angiotensin II receptor antagonists, NSAIDs (non steroidal anti-inflammatory medicines, e. g. aspirin or ibuprofen), heparin, immunosuppressives (e. g. cyclosporin or tacrolimus), and the antibiotic trimethoprim. • Diuretics ('water tablets '), especially if taken in high doses together with Kinzalmono, may lead to excessive loss of body water and low blood pressure (hypotension).

• The batches passed the Ph. Eur. potency test in pigs at 1/ 3 dose, which provides evidence of target animal efficacy. • The batches are formulated with a fixed quantity of bacteria, quantified using an approved and validated method. • The batches passed the test for target animal safety according to Ph. Eur monograph 0064. • The batches were commercial batches manufactured to the production methods and specification described in the MA. • The potencies of the two reference batches (9097 and 9861) are higher than the PEI reference serum and the reference vaccine batch 8500. • The MAH followed the correct SOP for replacement at the time the replacements were made.

The dose of INCRELEX should not be doubled to make up for one or more omitted doses. • To avoid engaging in any high-risk activities (such as vigorous physical activity) within 2 - 3 hours after dosing, particularly at the initiation of INCRELEX treatment, until a well-tolerated dose of INCRELEX has been established. • Instructions to change and rotate the site of injection for each injection to avoid the development of lipohypertrophy. • Instructions to report the onset or worsening of snoring that may indicate an increase in growth of tonsils and/ or adenoids following the beginning of treatment with INCRELEX. • To report the onset of severe headache blurred vision and associated nausea and vomiting to their physician. • To report any onset of a limp or complaint of hip or knee pain to their physician so it can be evaluated.