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2003 FDA批准的在美国市场化销售的28种药物
| 药品名 |
商标名 |
制药厂 |
药物分类 |
给药途径 |
FDA 分类a |
| Humira |
Adalimumabb |
Abbott |
抗关节炎 |
皮下注射 |
Sc |
| Fabrazyme |
Agalsidase beta |
Genzyme |
抗纤维化疾病 |
静脉注射 |
P, H, Vc |
| Amevive |
Alefacept |
Biogen |
抗牛皮癣 |
肌肉 |
Sb |
| Uroxatral |
Alfuzosin hydrochloride |
Sanofi-Synthélabo |
抗良性前聂腺增生 |
口服 |
1-S |
| Emend |
Aprepitant |
默克 |
抗呕吐 |
口服 |
1-P |
| Reyataz |
Atazanavir sulfate |
Bristol-Myers Squibb |
抗病毒 |
口服 |
1-P |
| Strattera |
Atomoxetine hydrochlorideb |
Lilly |
治疗多动症和注意力不集中 |
口服 |
1-S |
| Velcade |
Bortezomib |
Millennium |
抗癌症 |
静脉注射 |
1-P, H |
| Cubicin |
Daptomycin |
Cubist |
抗菌素 |
静脉注射 |
1-P |
| Raptiva |
Efalizumab |
Genentech; Xoma |
治疗牛皮癣 |
Subcutaneous |
Sc |
| Relpax |
Eletriptan hydrobromideb |
辉瑞 |
抗偏头痛 |
口服 |
1-S |
| Emtriva |
Emtricitabine |
Gilead Sciences |
抗病毒 |
口服 |
1-S |
| Fuzeon |
Enfuvirtide |
Roche; Trimeris |
抗病毒 |
Subcutaneous |
1-P, H |
| Inspra |
Eplerenonec |
辉瑞 |
治疗充血性心脏病和高血压 |
口服 |
1-S |
| Iressa |
Gefitinib |
AstraZeneca |
抗癌 |
口服 |
1-P, H |
| Extraneal |
Icodextrinb |
Baxter |
腹部透晰 |
Peritoneal |
1-S |
| Aldurazyme |
Laronidase |
Genzyme |
粘多糖病 |
静脉注射 |
P, Vc |
| Namenda |
Memantine hydrochloride |
Forest |
老年痴呆 |
口服 |
1-S, V |
| Solagé |
Mequinol/tretinoinb |
Galderma |
皮肤漂白 |
表皮 |
1, 4-S |
| Zavesca |
Miglustat |
Actelion |
Gaucher病(一种失算,震颤,失言等症状的神经性疾病) |
口服 |
1-S, V |
| Alinia |
Nitazoxanideb |
Romark |
抗寄生虫 |
口服 |
1-P, V |
| Xolair |
Omalizumab |
Genentech; Novartis |
抗哮喘 |
Subcutaneous |
Sc |
| Aloxi |
Palonosetron hydrochloride |
MGI Pharma |
抗呕吐剂 |
静脉注射 |
1-S |
| Somavert |
Pegvisomant |
辉瑞 |
肢端肥大症治疗 |
Subcutaneous |
1-P, V |
| Crestor |
Rosuvastatin calcium |
AstraZeneca |
抗高脂血症 |
口服 |
1-S |
| Cialis |
Tadalafil |
Lilly; ICOS |
勃起功能障碍 |
口服 |
1-S |
| Bexxar |
Tositumomab and iodine I-131 tositumomab |
Corixa; GlaxoSmithKline |
抗高脂血症 |
静脉注射 |
Pc |
| Levitra |
Vardenafil hydrochloride |
Bayer; GlaxoSmithKline |
勃起功能障碍 |
口服 |
1-S |
| a |
FDA classification of new drugs: 1 = new molecular entity; 4 =
combination product; P = priority review; S = standard review; H =
accelerated approval; V = designated orphan drug. |
| b |
Approved by FDA before 2003 but not marketed until 2003. |
| c |
A biological approved through an FDA procedure that does not assign a
numerical classification. |
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