Sananginas Overdose

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Sananginas warnings

Warnings are a mix of Precautions. Contraindications and interactions and serious harmful effects associated with the medicine intake. A diabetic or Hypertensive patient need to be warned about few drug interactions. A known hypersensitivity patient needs to be careful about the reactions or anaphylactic shock. A pregnant woman or a breastfeeding woman should be warned of certain medications. A Hepatitis [liver disease] patient or a cardiac patient should avoid few drugs.
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Caution is advised in patients with hyponatremia, severe hypotension, AV conduction abnormalities, respiratory depression after intoxication (eg

Barbiturates or psychotropic drugs), familial periodic paralysis, diabetes mellitus, advanced liver insufficiency, calcium-magnesium-ammonium- or therapy with potassium-sparing diuretics. monitor the acid-base balance, water balance, potassium and Magesiumausscheidung in urine, possibly pH value of serum

and ECG monitoring are required. At higher doses running ECG monitoring is required.

Sananginas precautions

Certain people who are very sick or very old or who are sensitive show an exacerbation of side effect of the drug which can turn dangerous at times. So, it is very important to remember the precautions while taking the medicine. Pregnancy and Breastfeeding are also special categories wherein extra care or precaution is needed when taking a drug. Few patients may have a hypersensitivity reaction to few medications, and that can be life-threatening rarely. Penicillin hypersensitivity is one example. Diarrhea, rashes are few other symptoms which need a watch. A patient with other co-existing diseases like liver disease, heart disease, kidney disease should take special precautions.

Chronic renal disease & other condition which impairs K & Mg excretion.

References

  1. EU Food Improvement Agents. "Aspartic acid: Commission Implementing Regulation (EU) No 872/2012 of 1 October 2012 adopting the list of flavouring substances provided for by Regulation (EC) No 2232/96 of the European Parliament and of the Council, introducing it in Annex I to Regulation (EC) No 1334/2008 of the European Parliament and of the Council and repealing Commission Regulation (EC) No 1565/2000 and Commission Decision 1999/217/EC Text with EEA relevance". http://eur-lex.europa.eu/legal-conte... (accessed September 17, 2018).

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Information checked by Dr. Sachin Kumar, MD Pharmacology

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