“Adverse Event”. Adverse Event means any unwanted or harmful medical occurrence in a patient or subject who is administered a Product, whether or not considered related to such Product, including any undesirable sign (including abnormal laboratory findings of clinical concern), symptom or disease temporally associated with the use of such Product.

“Adverse Event”1">. Adverse Event means any unwanted or harmful medical occurrence in a patient or subject who is administered 3">treatment using a Product, whether or not considered related to 5">such Product,5">Products, including any undesirable sign (including abnormal laboratory findings of clinical concern), symptom or disease temporally associated with the use of 7">such Product.7">Products.

“Adverse Event”1">. Adverse Event means any unwanted or harmful medical occurrence in a patient or subject who is administered a Product, whether or not considered related to such Product, including any undesirable sign (including abnormal laboratory findings of clinical concern)3">, symptom or disease temporally associated with the use of such Product.3">.

“Adverse Event”1">. Adverse Event means any 3">unwanted or harmful3">untoward medical occurrence in a 5">patient5">human clinical study subject or 7">subject7">in a patient who is administered a 9">Product,9">product, whether or not considered related to such 11">Product,11">product, including any undesirable sign (including abnormal laboratory findings of clinical concern), 13">symptom13">symptom, or disease15"> temporally associated with the use of 17">such Product.17">a product.

“Adverse Event”1">. Adverse Event means any 3">unwanted or harmful3">untoward medical occurrence in a 5">patient5">Clinical Trial subject or 7">subject7">patient who is administered a Product, whether or not considered related to such Product, including any undesirable sign (including abnormal laboratory findings of clinical concern), symptom or disease 9">temporally associated with the use of such Product.

“Adverse Event”1">. Adverse Event means any 3">unwanted or harmful3">untoward medical occurrence in a 5">patient5">human clinical trial subject or 7">subject7">in a patient who is administered a Product, whether or not considered related to 9">such Product, including9">the Product including, without limitation, any undesirable sign (including abnormal laboratory findings of clinical concern), symptom or disease 11">temporally associated with the use of such Product.

“Adverse Event”1">. Adverse Event means1"> shall mean any 3">unwanted or harmful3">untoward medical occurrence in a patient or 5">clinical investigation subject who is administered 7">the Product, but which does not necessarily have a 9">Product, whether or not considered related to such Product, including9">causal relationship with the treatment for which the Product is used. An “Adverse Event” can include any 11">undesirable11">unfavorable and unintended sign (including 13">an abnormal laboratory 15">findings of clinical concern)15">finding), symptom or disease temporally associated with the use of 17">such17">the Product, whether or not related to the Product.19"> A pre-existing condition that worsened in severity after administration of the Product would be considered an “Adverse Event”.

“Adverse Event”1">. Adverse Event means1"> shall mean any 3">unwanted or harmful3">untoward medical occurrence in a patient or 5">clinical investigation subject who is administered 7">the Product, but which does not necessarily have a 9">Product, whether or not considered related to such Product, including9">causal relationship with the treatment for which the Product is used. An “Adverse Event” can include any 11">undesirable11">unfavorable and unintended sign (including 13">an abnormal laboratory 15">findings of clinical concern)15">finding), symptom or disease temporally associated with the use of 17">such17">the Product, whether or not related to the Product.19"> A pre- existing condition that worsened in severity after administration of the Product would be considered an “Adverse Event”.

“Adverse Event”1">. Adverse Event means any 3">unwanted or harmful3">untoward medical occurrence in a patient or 5">human clinical investigation subject 7">who is administered9"> a Product, whether or not considered related to such Product, including 11">any undesirable sign (including abnormal laboratory findings of clinical concern), symptom or disease temporally associated11">occurrences that do not necessarily have a causal relationship with 13">the use of such Product.