This was consistent with the observations in animal studies.

In animal studies TachoSil shows a progressive biodegradation.

Tetranor iloprost is pharmacologically inactive as shown in animal experiments.

Animal studies have shown excretion of lansoprazole in milk.

Animal studies have shown excretion of lansoprazole in milk.

Studies in animals have shown reproductive toxicity (see section 5.3).

Intestinal metaplasia has been found in animal studies on rats.

Loratadine was not teratogenic in animal studies.

Animal studies suggest a toxic effect in early pregnancy (see section 5.3).

Animal studies have shown excretion of sitagliptin in breast milk.

Intestinal metaplasia has been found in animal studies on rats.

Studies in animals have shown reproductive toxicity (see section 5.3).

Only limited data from animal studies are available regarding the placental transfer (see section 5.3).

Only limited data from animal studies are available regarding the placental transfer (see section 4.6).

Animal studies indicate that leflunomide or its metabolites pass into breast milk.

Animal studies suggest a toxic effect in early pregnancy (see section 5.3).

Pregnancy and lactation Loratadine was not teratogenic in animal studies.

Pregnancy and lactation Loratadine was not teratogenic in animal studies.

And, and, and there are a lot more animal studies that I could talk about.

Foetal growth restriction was apparent in animal studies with pioglitazone.

In animal studies, risperidone and 9 hydroxy risperidone are excreted in the milk.

Harmful effects have been seen in reproductive toxicological animal studies.

And this was really interesting, because it's sort of opposite and parallel of what some animal studies have shown.

These recommendations, based on physiological and observational studies, proved profoundly misleading.

Studies in animals have shown reproductive and developmental toxicity (see section 5.3).

Animal studies do not indicate direct harmful effects with respect to pregnancy, embryonal foetal development, parturition or postnatal development.

163 Animal studies do not indicate direct harmful effects with respect to pregnancy, embryonal foetal development, parturition or postnatal development.

175 Animal studies do not indicate direct harmful effects with respect to pregnancy, embryonal foetal development, parturition or postnatal development.

187 Animal studies do not indicate direct harmful effects with respect to pregnancy, embryonal foetal development, parturition or postnatal development.

199 Animal studies do not indicate direct harmful effects with respect to pregnancy, embryonal foetal development, parturition or postnatal development.

The carcinogenic potential of darbepoetin alfa has not been evaluated in long term animal studies.

Adverse reactions observed in animal studies with possible clinical relevance were as follows

Animal studies with similar substances have shown reproductive toxicity (see section 5.3).

Animal studies do not indicate direct harmful effects with respect to pregnancy, parturition or postnatal development.

The carcinogenic potential of darbepoetin alfa has not been evaluated in long term animal studies.

Bolus intravenous administration of tigecycline has been associated with a histamine response in animal studies.

Animal studies have shown that calcitonin is primarily metabolised via proteolysis in the kidney following parenteral administration.

Animal studies have shown that elcatonin is primarily metabolised via proteolysis in the kidney following parenteral administration.

Animal studies showed that daptomycin is not absorbed to any significant extent after oral administration.

Animal studies showed that daptomycin is not absorbed to any significant extent after oral administration.

Animal studies have shown toxicity to parturition, peri and post natal development (see section 5.3).

Animal studies have shown that calcitonin is primarily metabolised via proteolysis in the kidney following parenteral administration.

Animal studies are insufficient with respect to pregnancy (see section 5.3).

The carcinogenic potential of darbepoetin alfa has not been evaluated in long term animal studies.

Cytochromes P450 CYP1A2 and P450 CYP2D6 contribute to the formation of the N desmethyl and 2 hydroxymethyl metabolites, both exhibited significantly less in vivo pharmacological activity than olanzapine in animal studies.