Examples of 'toxicity see' in a sentence

Meaning of "toxicity see"

Toxicity see is not a commonly used phrase in English. It might be a misinterpretation or a typo. There is no specific meaning associated with this phrase

How to use "toxicity see" in a sentence

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toxicity see
Patients continued therapy until disease progression or unacceptable toxicity see section.
Mammalian toxicity see point 2.
Animal studies are insufficient with respect to reproductive toxicity see section.
Studies in animals have shown reproductive toxicity see Section 5.3 Preclinical safety data.
Animal studies on emtricitabine and tenofovir disoproxil do not indicate reproductive toxicity see section 5.3.
Animal studies do not indicate reproductive toxicity see Section 5.3 - Preclinical safety data.
Rat pups exposed pre and post-natally to amprenavir and fosamprenavir showed developmental toxicity see section 5.3.
Studies in animals have shown reproductive toxicity see PART II, TOXICOLOGY.
Animal studies are insufficient with respect to developmental toxicity see section 5.3.
Animal studies provide limited evidence of reproductive toxicity see Section 5.3 Preclinical safety data.
Dose modifications were allowed for improving activity or management of toxicity see section 4.2.
Terrestrial vertebrates Mammalian toxicity see point 2.
A study in rabbits did not indicate reproductive or developmental toxicity see section 5.3.
Studies in animals have shown reproductive toxicity see sections 5.3.
However, these are insufficient with respect to human reproductive toxicity see section 5.3.
Monitor for signs of zidovudine toxicity see section 4.8.
Animal studies have revealed minimal developmental toxicity see section 5.3.
Studies in animals have shown reproductive toxicity see Fertility.
Studies in animals have shown reproduction toxicity see section 5.3.
Animal studies do not indicate reproductive toxicity see section 5.3.
Studies in animals have shown developmental toxicity see section 5.3.
Studies in rabbits have shown reproductive toxicity see section 5.3.
Studies in animals have shown embryofoetal toxicity see section 5.3.
Studies in animals have shown some embryologic toxicity see section 5.3.
Studies of pioglitazone in animals have shown reproductive toxicity see section 5.3.
Patients should be monitored for symptoms of pulmonary toxicity see section 4.2.
Animal reproduction studies have shown reproductive toxicity see section 5.3.
Studies in rats have shown some reproductive toxicity see section 5.3.
Studies in animals have shown some reproductive toxicity see section 5.3.
Not recommended due to the potential for hepatic toxicity see section 4.3.
Animal studies could not exclude potential developmental toxicity see section 5.3.
Animal studies are not available with respect to reproductive toxicity see section 5.3.
Studies in animals have shown reproductive and developmental toxicity see section 5.3.
Studies with telmisartan in animals have shown reproductive toxicity see section 5.3.
Studies in animals with canagliflozin have shown reproductive toxicity see section 5.3.
Studies with raltegravir in animals have shown reproductive toxicity see section 5.3.
Animal studies have shown a possible link to reproductive toxicity see section 5.3.
Animal studies are insufficient with respect to human reproductive toxicity see section 5.3.
Treatment may be reinstituted following resolution of the haematological toxicity see section 4.2.
Studies in animals using parenteral administration have shown reproductive toxicity see section 5.3.
Studies in animals administered adefovir intravenously have shown reproductive toxicity see section 5.3.
Animal studies with similar substances have shown reproductive toxicity see section 5.3.
If overdose occurs the patient must be monitored for evidence of toxicity see section 4.8.
Traditional non-clinical studies are insufficient with respect to reproductive toxicity see section 5.3.
In studies conducted in rabbits, bazedoxifene alone has shown reproductive toxicity see section 5.3.
Few pre-clinical data are available with respect to reproductive toxicity see section 5.3.
Embryotoxic effects have been shown at doses in the range of maternal toxicity see section 5.3.
The recommended dose should be reduced in patients with haematological toxicity see section 4.2.
Animal reproduction studies with zoledronic acid have shown reproductive toxicity see section 5.3.
Studies with abacavir and lamivudine in animals have shown reproductive toxicity see section 5.3.

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Examples of using See
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Examples of using Toxicity
Adequate chronic toxicity data not available
Toxicity is a measure of how harmful or poisonous a pesticide is
No clinical signs of toxicity were observed at any dose
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