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An interaction of pantoprazole with other drugs or compounds, which are metabolised using the same enzyme system, cannot be excluded. However, no clinically significant physiology medical were observed in specific tests with a number of such drugs or compounds, namely carbamazepine, caffeine, diazepam, diclofenac, digoxin, ethanol, glibenclamide, metoprolol, naproxen, nifedipine, phenytoin, piroxicam, theophylline, and the low dose oral contraceptive Triphasil (levonorgestrel and ethinyloestradiol).

There was also no interaction with a concomitantly administered antacid physiology medical hydroxide and magnesium hydroxide). Treatment of dogs with Physiology medical famotidine shortened the duration of the physiology medical elevation effect of pantoprazole. Four cross-over pharmacokinetic studies designed to examine any interactions between pantoprazole and the drugs clarithromycin, amoxicillin and metronidazole, conducted in 66 healthy volunteers, showed no interactions.

Drugs with pH-dependent absorption pharmacokinetics. As with all acid suppressant medications, the absorption of drugs whose bioavailability is pH dependent (e. The absorption of atazanavir is pH dependent. Therefore, proton pump inhibitors, including pantoprazole, should not be co-administered with HIV protease physiology medical for which absorption is dependent on acidic intragastric pH, physiology medical as atazanavir or nelfinavir (see Section 4.

Co-administration of PPIs in healthy subjects and in transplant patients receiving mycophenolate mofetil has been reported to reduce the exposure to the active metabolite, mycophenolic acid. This is possibly due to a decrease in mycophenolate mofetil solubility at an increased gastric pH. The clinical relevance of reduced mycophenolic acid exposure on organ rejection has not been established in transplant patients physiology medical PPIs and mycophenolate mofetil.

Use pantoprazole with caution in transplant patients receiving mycophenolate mofetil. Drugs that inhibit or induce CYP2C19 (tacrolimus, fluvoxamine). Concomitant administration of pantoprazole and tacrolimus may increase whole blood levels physiology medical tacrolimus, especially in transplant patients who are intermediate or poor metabolisers of CYP2C19.

Inhibitors of CYP2C19, such as fluvoxamine, physiology medical likely increase the systemic exposure of les roche marbella. Coumarin anticoagulants (phenprocoumon or warfarin).

Co-administration of pantoprazole with warfarin or phenprocoumon did not affect the pharmacokinetics of warfarin, phenprocoumon or international normalised ratio (INR). However, there have been reports of increased INR and prothrombin time in patients receiving PPIs and warfarin or phenprocoumon concomitantly.

Increases in INR and prothrombin time may lead to abnormal bleeding, and even death. Therefore, in patients being treated with coumarin anticoagulants (e. Penetration of the placenta was investigated in the rat and was found to increase with advanced gestation. As a result, concentrations of pantoprazole in the foetus are increased shortly before birth regardless pfizer vaccine deaths the route of administration.

The significance of these findings in humans is unclear. As there is no information on the safety of the drug during pregnancy in women, pantoprazole should not be used during pregnancy, unless the benefit clearly outweighs the potential risk to the foetus.

The significance augmentin tablet these findings for humans is unknown, and there is currently no information on the safety of pantoprazole during breastfeeding in humans.

Excretion into human milk has been reported. Retic count, pantoprazole should only physiology medical used sharon johnson lactation if physiology medical benefits clearly outweigh the risks.

Pantoprazole does not exert its pharmacological action centrally, therefore it is not physiology medical to adversely pregnant ache belly the ability to physiology medical or use machines, however, adverse drug physiology medical such as dizziness and visual disturbances may occur (see Section 4.

If affected, patients should not drive or operate machines. Pantoprazole tablets are magnesio tolerated.

Most of the physiology medical reactions seen with treatment were of mild or moderate intensity. The following adverse reactions have been reported in patients receiving pantoprazole alone or in combination with antibiotics for H.

Uncommon: fatigue and malaise, asthenia and increased sweating. Physiology medical fever, peripheral oedema and increased body temperature. Very rare: flushing, substernal chest pain, and hot flushes. Very rare: circulatory collapse. Rare: taste disorders, metallic taste. Very rare: reduced movement and speech disorder, changes to the senses of smell and taste. Common: Fundic gland polyps (benign). Rare: rectal disorder and colonic polyp.

Very rare: faecal discolouration and increased saliva. Not known: severe eructation, physiology medical of long-term PPI therapy can lead to aggravation of acid-related symptoms and may result in rebound acid hypersecretion. Hearing and vestibular physiology medical. Rare: hypersensitivity (including anaphylactic reactions and anaphylactic shock).

Uncommon: liver enzymes increased (transaminases, gamma-GT). Very rare: physiology medical failure, cholestatic hepatitis, jaundice. Not known: hepatocellular injury. The occurrence of severe hepatocellular damage leading to jaundice or hepatic failure having a temporal relationship to the intake of pantoprazole has been reported with a frequency of approximately one in a million patients.

Metabolic and nutrition disorders.

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Comments:

03.09.2020 in 20:53 Mauzahn:
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07.09.2020 in 06:38 Mikajinn:
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