XELODA TABLETS 150 mg সিঙ্গাপুর - ইংরেজি - HSA (Health Sciences Authority)

xeloda tablets 150 mg

dksh singapore pte. ltd. - capecitabine - tablet, film coated - 150 mg - capecitabine 150 mg

XELODA TABLETS 500 mg সিঙ্গাপুর - ইংরেজি - HSA (Health Sciences Authority)

xeloda tablets 500 mg

dksh singapore pte. ltd. - capecitabine - tablet, film coated - 500 mg - capecitabine 500 mg

DORMICUM TABLET 7.5 mg সিঙ্গাপুর - ইংরেজি - HSA (Health Sciences Authority)

dormicum tablet 7.5 mg

roche singapore pte. ltd. - midazolam maleate 10.2mg eqv. to midazolam - tablet, film coated - 7.5mg

DORMICUM TABLET 15 mg সিঙ্গাপুর - ইংরেজি - HSA (Health Sciences Authority)

dormicum tablet 15 mg

dksh singapore pte. ltd. - midazolam maleate 20.40 mg eqv. to midazolam - tablet, film coated - 15 mg - midazolam maleate 20.40 mg eqv. to midazolam 15 mg

Dormicum 15 mg Film-Coated Tablet ফিলিপাইন - ইংরেজি - FDA (Food And Drug Administration)

dormicum 15 mg film-coated tablet

zuellig pharma corporation; distributor: zuellig pharma corporation - midazolam - film-coated tablet - 15 mg

Dormicum 15mg Tablet ফিলিপাইন - ইংরেজি - FDA (Food And Drug Administration)

dormicum 15mg tablet

roche (philippines) inc.; distributor: zuellig pharma corporation - midazolam (as maleate) - tablet - 15mg

ANASCORP (centruroides (scorpion) immune f(ab)2- equine injection, powder, lyophilized, for solution মার্কিন যুক্তরাষ্ট্র - ইংরেজি - NLM (National Library of Medicine)

anascorp (centruroides (scorpion) immune f(ab)2- equine injection, powder, lyophilized, for solution

rare disease therapeutics, inc - centruroides fab2 antivenin (equine) (unii: dda050fcea) (centruroides fab2 antivenin (equine) - unii:dda050fcea) - centruroides fab2 antivenin (equine) 24 mg in 1 ml - anascorp® [centruroides (scorpion) immune f(ab')2 (equine) injection] is an equine-derived antivenom indicated for treatment of patients with clinical signs of scorpion envenomation. none. risk summary animal reproduction studies have not been conducted with anascorp. it is also not known whether anascorp can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. anascorp should be given to a pregnant woman only if clearly needed. risk summary it is not known whether anascorp is excreted in human breast milk. because many drugs are excreted in human milk, caution should be exercised when anascorp is administered to a nursing woman. seventy-eight percent of the patients enrolled in the clinical studies were pediatrics subjects(1204/1534), with ages ranging from less than one month to 18.7 years of age. patient age groups were as follows: < 2 years of age, 29%, 2 to 5 years, 37%, 5 to 18 years, 34%. the efficacy and safety