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Sanilvudine adverse events reported to FDA.

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Summary

FDA Adverse Reports: 3. View All

Sanilvudine FDA safety alerts: No

Reported deaths: 3

Reported hospitalizations: 3

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Often additional risks of using a medication, such as Sanilvudine, become known after product is used by a larger number of patients, for a longer period of time, and by patients with different health characteristics from those studied before drug approval. This page allows You to Find answers and discuss health symptoms with other Sanilvudine users, Learn more about unwanted side effects & find ways to reduce them. Browse Sanilvudine Adverse Reports reported to FDA and participate in Sanilvudine discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Sanilvudine. You can also Post a question to users community or Ask a Doctor. PatientsVille.com is Your Complete Guide to all common, undocumented and undisclosed side effects associated with drugs and vaccines. Browse More Drug Reports Here: A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z

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Sanilvudine Adverse Effect Reports (FDA)

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6620506-4 | Bone Marrow Failure, Gastric Ulcer Haemorrhage, Nausea, Pneumocystis Jiroveci Pneumonia, Renal Failure Acute, Respiratory Failure, Seminoma
on Mar 01, 2010 Male patient from JAPAN , 48 years of age, was diagnosed with acquired immunodeficiency syndrome, prophylaxis, seminoma and was treated with Sanilvudine (View Usage). Patient experienced the following unwanted or unexpected effects: bone marrow failure, gastric ulcer haemorrhage, nausea (What is nausea?), pneumocystis jiroveci pneumonia, renal failure acute, respiratory failure, seminoma. Sanilvudine dosage: . During the same period patient was treated with SULFAMETHOXAZOLE AND TRIMETHOPRIM (View Sulfamethoxazole And Trimethoprim Review and Sulfamethoxazole And Trimethoprim Label ), RANDA (On Days 1 To 5, Continuous Infusion) (View Randa Review and Randa Label ), BLEOMYCIN HCL (1 Dosageform = 30mg/body Form = Inj On Days 2, 9, 16) (View Bleomycin Hcl Review and Bleomycin Hcl Label ), LASTET (On Days 1-5) (View Lastet Review and Lastet Label ), LOPINAVIR AND RITONAVIR (View Lopinavir And Ritonavir Review and Lopinavir And Ritonavir Label ), LAMIVUDINE (Form = Tabs) (View Lamivudine Review and Lamivudine Label ), FLUCONAZOLE (View Fluconazole Review and Fluconazole Label ). Patient was hospitalized.

6587975-X | Bone Marrow Failure, Gastric Ulcer Haemorrhage, Nausea, Pneumocystis Jiroveci Pneumonia, Renal Failure Acute, Respiratory Failure, Seminoma
Patient was taking Sanilvudine (View Usage). Patient had the following side effects: bone marrow failure, gastric ulcer haemorrhage, nausea (What is nausea?), pneumocystis jiroveci pneumonia, renal failure acute, respiratory failure, seminoma on Feb 09, 2010 from JAPAN Additional patient health information: Male patient , 48 years of age, was diagnosed with acquired immunodeficiency syndrome, prophylaxis, seminoma and. Sanilvudine dosage: . During the same period patient was treated with SULFAMETHOXAZOLE AND TRIMETHOPRIM (View Sulfamethoxazole And Trimethoprim Review and Sulfamethoxazole And Trimethoprim Label ), CISPLATIN (On Days 1 To 5, Continuous Infusion) (View Cisplatin Review and Cisplatin Label ), BLEOMYCIN HCL (1 Dosageform = 30mg/body Form = Inj On Days 2, 9, 16) (View Bleomycin Hcl Review and Bleomycin Hcl Label ), ETOPOSIDE (On Days 1-5) (View Etoposide Review and Etoposide Label ), LOPINAVIR/RITONAVIR (View Lopinavir/ritonavir Review and Lopinavir/ritonavir Label ), LAMIVUDINE (Form = Tabs) (View Lamivudine Review and Lamivudine Label ), FLUCONAZOLE (View Fluconazole Review and Fluconazole Label ). Patient was hospitalized.

6566033-4 | Bone Marrow Failure, Gastric Ulcer Haemorrhage, Nausea, Pneumocystis Jiroveci Pneumonia, Renal Failure Acute, Respiratory Failure, Seminoma
Adverse event was reported on Jan 20, 2010 by a Male patient taking Sanilvudine (View Usage) (Dosage: ) was diagnosed with acquired immunodeficiency syndrome, seminoma, prophylaxis and. Location: JAPAN , 48 years of age, After Sanilvudine was administered, patient had the following side effects: bone marrow failure, gastric ulcer haemorrhage, nausea (What is nausea?), pneumocystis jiroveci pneumonia, renal failure acute, respiratory failure, seminoma. During the same period patient was treated with BRIPLATIN (On Days 1 To 5, Continuous Infusion) (View Briplatin Review and Briplatin Label ), SULFAMETHOXAZOLE AND TRIMETHOPRIM (View Sulfamethoxazole And Trimethoprim Review and Sulfamethoxazole And Trimethoprim Label ), BLEOMYCIN HCL (1 Dosageform = 30mg/body Form = Inj On Days 2, 9, 16) (View Bleomycin Hcl Review and Bleomycin Hcl Label ), ETOPOSIDE (On Days 1-5) (View Etoposide Review and Etoposide Label ), LOPINAVIR/RITONAVIR (View Lopinavir/ritonavir Review and Lopinavir/ritonavir Label ), LAMIVUDINE (Form = Tabs) (View Lamivudine Review and Lamivudine Label ), FLUCONAZOLE (View Fluconazole Review and Fluconazole Label ). Patient was hospitalized.


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To find out about documented side effects or safety concerns read either the drug label or the drug's package insert. You may also want to speak with your pharmacist or healthcare provider. All medicines have benefits and risks. The risks are the chances that something unwanted or unexpected could happen to you when you use them. You can protect yourself by searching summaries of recent safety alerts, adverse reports. Sometimes there are risks that only come to light after a medical product gets on the market and is used in a larger number of patients, for a longer period of time, and in patients whose health characteristics are different from those of the patients studied before approval.

Be aware of the following potential Sanilvudine risks to be aware of: 1. Watch for any Serious adverse events, such as life-threatening situation, which can require an admission to hospital or longer-than-expected hospital stay, permanent disability, birth defect, miscarriage, stillbirth, or birth with serious disease requires medical care to prevent permanent damage
2. Any potential Sanilvudine quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Sanilvudine use error: mixing up products with similar drug names or packaging, taking wrong dose of a drug because of confusing dosing instructions on label
4. When applicable, Problems with different manufacturer of same medicine: not getting same results from a generic drug as a brand name drug, or from another generic

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