Watsons One Step Ovulation Test Singapore - English - HSA (Health Sciences Authority)

watsons one step ovulation test

watson's personal care stores pte ltd - obstetrics & gynaecology - a qualitative test used to predict when there is a luteinizing hormone (lh) surge, and in turn, when you are likely to ovulate. for in vitro self test use only. for external use only.

Watsons One Step Pregnancy Planning Kit Singapore - English - HSA (Health Sciences Authority)

watsons one step pregnancy planning kit

watson's personal care stores pte ltd - obstetrics & gynaecology - a qualitative test used to detect lutenizing hormone and a rapid test for detection of pregnancy.

Watsons One Step Pregnancy Test Singapore - English - HSA (Health Sciences Authority)

watsons one step pregnancy test

watson's personal care stores pte ltd - obstetrics & gynaecology - it is a qualitative testing to detect the presence of human chorionic gonadotropin (hcg) in urine to screen for a pregnancy. it is a rapid pregnancy test that can be done by yourself easily and used from the day you missed your period.

naproxen- Naproxen tablet United States - English - NLM (National Library of Medicine)

naproxen- naproxen tablet

watson labs - naproxen (unii: 57y76r9atq) (naproxen - unii:57y76r9atq) - tablet - 250 mg - carefully consider the potential benefits and risks of naproxen and other treatment options before deciding to use naproxen. use the lowest effective dose for the shortest duration consistent with individual patient treatment goals (see warnings). naproxen tablets are indicated: - for relief of mild to moderate pain for relief of mild to moderate pain - for relief of signs and symptoms of juvenile arthritis for relief of signs and symptoms of juvenile arthritis - for relief of the signs and symptoms of rheumatoid arthritis for relief of the signs and symptoms of rheumatoid arthritis - for relief of the signs and symptoms of osteoarthritis for relief of the signs and symptoms of osteoarthritis - for treatment of primary dysmenorrhea for treatment of primary dysmenorrhea - for acute or long-term use in the relief of signs and symptoms of the following: ankylosing spondylitis acute painful shoulder (acute subacromial bursitis/supraspinatus tendinitis) acute gouty arthritis for acute or long-

BUPROPION HYDROCHLORIDE tablet, film coated, extended release United States - English - NLM (National Library of Medicine)

bupropion hydrochloride tablet, film coated, extended release

aphena pharma solutions - tennessee, llc - bupropion hydrochloride (unii: zg7e5poy8o) (bupropion - unii:01zg3tpx31) - bupropion hydrochloride 100 mg - bupropion hydrochloride extended-release tablets (sr) are indicated for the treatment of major depressive disorder. the efficacy of bupropion in the treatment of a major depressive episode was established in two 4-week controlled trials of depressed inpatients and in one 6-week controlled trial of depressed outpatients whose diagnoses corresponded most closely to the major depression category of the apa diagnostic and statistical manual (dsm) (see clinical pharmacology). a major depressive episode (dsm-iv) implies the presence of 1) depressed mood or 2) loss of interest or pleasure; in addition, at least 5 of the following symptoms have been present during the same 2-week period and represent a change from previous functioning: depressed mood, markedly diminished interest or pleasure in usual activities, significant change in weight and/or appetite, insomnia or hypersomnia, psychomotor agitation or retardation, increased fatigue, feelings of guilt or worthlessness, slowed thinking or impaired concentration, a

BUPROPION HYDROCHLORIDE tablet, film coated, extended release United States - English - NLM (National Library of Medicine)

bupropion hydrochloride tablet, film coated, extended release

aphena pharma solutions - tennessee, llc - bupropion hydrochloride (unii: zg7e5poy8o) (bupropion - unii:01zg3tpx31) - bupropion hydrochloride extended-release tablets (sr) are indicated for the treatment of major depressive disorder. the efficacy of bupropion in the treatment of a major depressive episode was established in two 4-week controlled trials of depressed inpatients and in one 6-week controlled trial of depressed outpatients whose diagnoses corresponded most closely to the major depression category of the apa diagnostic and statistical manual (dsm) (see clinical pharmacology). a major depressive episode (dsm-iv) implies the presence of 1) depressed mood or 2) loss of interest or pleasure; in addition, at least 5 of the following symptoms have been present during the same 2-week period and represent a change from previous functioning: depressed mood, markedly diminished interest or pleasure in usual activities, significant change in weight and/or appetite, insomnia or hypersomnia, psychomotor agitation or retardation, increased fatigue, feelings of guilt or worthlessness, slowed thinking or impaired concentration, a

HYDROCODONE ACETAMINOPHEN- hydrocodone, acetaminophen tablet United States - English - NLM (National Library of Medicine)

hydrocodone acetaminophen- hydrocodone, acetaminophen tablet

redpharm drug inc. - hydrocodone bitartrate (unii: no70w886kk) (hydrocodone - unii:6yks4y3wq7), acetaminophen (unii: 362o9itl9d) (acetaminophen - unii:362o9itl9d) - hydrocodone bitartrate 7.5 mg - indications and usage hydrocodone bitartrate and acetaminophen tablets are indicated for the relief of moderate to moderately severe pain. contraindications this product should not be administered to patients who have previously exhibited hypersensitivity to hydrocodone or acetaminophen. patients known to be hypersensitive to other opioids may exhibit cross-sensitivity to hydrocodone pediatric use safety and effectiveness in pediatric patients have not been established. geriatric use clinical studies of hydrocodone bitartrate and acetaminophen tablets did not include sufficient numbers of subjects aged 65 and over to determine whether they respond differently from younger subjects. other reported clinical experience has not identified differences in responses between the elderly and younger patients. in general, dose selection for an elderly patient should be cautious, usually starting at the low end of the dosing range, reflecting the greater frequency of decreased hepatic, renal, or cardiac

BUPROPION HYDROCHLORIDE tablet, film coated, extended release United States - English - NLM (National Library of Medicine)

bupropion hydrochloride tablet, film coated, extended release

stat rx usa llc - bupropion hydrochloride (unii: zg7e5poy8o) (bupropion - unii:01zg3tpx31) - bupropion hydrochloride 100 mg - bupropion hydrochloride extended-release tablets (sr) are indicated for the treatment of major depressive disorder. the efficacy of bupropion in the treatment of a major depressive episode was established in two 4-week controlled trials of depressed inpatients and in one 6-week controlled trial of depressed outpatients whose diagnoses corresponded most closely to the major depression category of the apa diagnostic and statistical manual (dsm) (see clinical pharmacology). a major depressive episode (dsm-iv) implies the presence of 1) depressed mood or 2) loss of interest or pleasure; in addition, at least 5 of the following symptoms have been present during the same 2-week period and represent a change from previous functioning: depressed mood, markedly diminished interest or pleasure in usual activities, significant change in weight and/or appetite, insomnia or hypersomnia, psychomotor agitation or retardation, increased fatigue, feelings of guilt or worthlessness, slowed thinking or impaired concentration, a

BUPROPION HYDROCHLORIDE tablet, film coated, extended release United States - English - NLM (National Library of Medicine)

bupropion hydrochloride tablet, film coated, extended release

rebel distributors corp - bupropion hydrochloride (unii: zg7e5poy8o) (bupropion - unii:01zg3tpx31) - bupropion hydrochloride 100 mg - bupropion hydrochloride extended-release tablets (sr) are indicated for the treatment of major depressive disorder. the efficacy of bupropion in the treatment of a major depressive episode was established in two 4-week controlled trials of depressed inpatients and in one 6-week controlled trial of depressed outpatients whose diagnoses corresponded most closely to the major depression category of the apa diagnostic and statistical manual (dsm) (see clinical pharmacology). a major depressive episode (dsm-iv) implies the presence of 1) depressed mood or 2) loss of interest or pleasure; in addition, at least 5 of the following symptoms have been present during the same 2-week period and represent a change from previous functioning: depressed mood, markedly diminished interest or pleasure in usual activities, significant change in weight and/or appetite, insomnia or hypersomnia, psychomotor agitation or retardation, increased fatigue, feelings of guilt or worthlessness, slowed thinking or impaired concentration, a