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This is an index of reports of adverse events (side effects, adverse reactions, etc.) related to Viread (Tenofovir Disoproxil). Click on the relevant link below to view a selection of reports according to the event's seriousness level and/or the nature of the side effect / adverse reaction. Or scroll down to view a sample of recent reports further on this page.
Our database includes reports from Jan 2007 to Dec 2007. The information is not vetted and should not be cosidered as verified clinical evidence.
All cases (246)
Cases resulting in a serious event (244)
Cases resulting in death (26)
Cases resulting in life threatening events (18)
Cases resulting in hospitalization (107)
Cases resulting in disability (21)
Cases resulting in other serious reactions (109)
Below is a sample of reports where side effects / adverse reactions may be related to Viread (Tenofovir Disoproxil). For a complete list and/or a specific selection of reports, please use the links in the index above.
Adverse event in receiving Viread (Tenofovir Disoproxil)
Reported by a individual with unspecified qualification from Italy on 2007-10-30
Patient:
Adverse reactions / side effects: Beta 2 Microglobulin Urine Increased
Suspect drug(s):
Viread (Tenofovir Disoproxil)
Adverse event in receiving Viread (Tenofovir Disoproxil)
Reported by a individual with unspecified qualification from Italy on 2007-10-30
Patient:
Adverse reactions / side effects: Beta 2 Microglobulin Urine Increased
Suspect drug(s):
Viread (Tenofovir Disoproxil)
Adverse event in receiving Viread (Tenofovir Disoproxil)
Reported by a individual with unspecified qualification from Italy on 2007-10-30
Patient:
Adverse reactions / side effects: Beta 2 Microglobulin Urine Increased
Suspect drug(s):
Viread (Tenofovir Disoproxil)
Adverse event in receiving Viread (Tenofovir Disoproxil)
Reported by a individual with unspecified qualification from Italy on 2007-10-30
Patient:
Adverse reactions / side effects: Beta 2 Microglobulin Urine Increased
Suspect drug(s):
Viread (Tenofovir Disoproxil)
Adverse event in receiving Viread (Tenofovir Disoproxil)
Reported by a individual with unspecified qualification from Italy on 2007-10-30
Patient:
Adverse reactions / side effects: Beta 2 Microglobulin Urine Increased
Suspect drug(s):
Viread (Tenofovir Disoproxil)
Adverse event in receiving Viread (Tenofovir Disoproxil)
Reported by a individual with unspecified qualification from Italy on 2007-10-30
Patient:
Adverse reactions / side effects: Beta 2 Microglobulin Urine Increased
Suspect drug(s):
Viread (Tenofovir Disoproxil)
Adverse event in receiving Viread (Tenofovir Disoproxil)
Reported by a individual with unspecified qualification from Italy on 2007-10-30
Patient:
Adverse reactions / side effects: Beta 2 Microglobulin Urine Increased
Suspect drug(s):
Viread (Tenofovir Disoproxil)
Adverse event in male receiving Viread (Tenofovir Disoproxil)
Reported by a physician from United Kingdom on 2007-10-29
Patient: male, weighing 73.0 kg (160.6 pounds)
Adverse reactions / side effects: Weight Decreased, Abdominal Pain, Fanconi Syndrome Acquired, Blood Chloride Increased, Polyuria, Acidosis, Thirst, Blood Phosphorus Decreased, Malaise, Glycosuria, Proteinuria, Blood Bicarbonate Increased, Blood Creatinine Increased
Suspect drug(s):
Viread (Tenofovir Disoproxil)
Other drugs received by patient: Didanosine; Kaletra; CO-Trimoxazole
Adverse event in 51 year old male receiving Viread (Tenofovir Disoproxil)
Reported by a physician from Thailand on 2007-10-26
Patient: 51 year old male, weighing 55.0 kg (121.0 pounds)
Adverse reactions / side effects: Renal Failure Acute
Adverse event resulted in: life threatening event
Suspect drug(s):
Viread (Tenofovir Disoproxil)
Other drugs received by patient: Lamivudine; Lopinavir and Ritonavir; Cotrimoxazole; Fluconazole; Ethambutol HCL; Azithromycin; Isoniazid; Ciprofloxacin; Prednisolone
Adverse event in 52 year old female receiving Viread (Tenofovir Disoproxil)
Reported by a physician from United Kingdom on 2007-10-24
Patient: 52 year old female
Adverse reactions / side effects: Overdose, Suicide Attempt
Suspect drug(s):
Viread (Tenofovir Disoproxil)
Adverse event in 24 year old male receiving Viread (Tenofovir Disoproxil)
Reported by a individual with unspecified qualification from United States on 2007-10-24
Patient: 24 year old male
Adverse reactions / side effects: Abdominal Pain, Weight Decreased, Gastrointestinal Motility Disorder, Hepatomegaly, Vomiting, Nausea, Gastritis
Suspect drug(s):
Viread
Etibi
Zithromax
Reyataz
Videx
Lamivudine
Kaletra
Bactrim
Adverse event in female receiving Viread (Tenofovir Disoproxil)
Reported by a physician from Sweden on 2007-10-23
Patient: female
Adverse reactions / side effects: Pregnancy, Ultrasound Antenatal Screen Abnormal
Suspect drug(s):
Viread (Tenofovir Disoproxil)
Other drugs received by patient: 3TC
Adverse event in male receiving Viread (Tenofovir Disoproxil)
Reported by a physician on 2007-10-23
Patient: male, weighing 89.0 kg (195.8 pounds)
Adverse reactions / side effects: Drug Resistance
Suspect drug(s):
Viramune
Dosage: 200mg during 14 days, thereafter 400mg
Administration route: Oral
Indication: HIV Infection
Start date: 2007-05-21
End date: 2007-07-30
Viread
Administration route: Oral
Indication: HIV Infection
Start date: 2007-05-21
Epivir
Administration route: Oral
Indication: HIV Infection
Start date: 2007-05-21
End date: 2007-07-30
Other drugs received by patient: Glucovance; Eusaprim; Eusaprim
Adverse event in male receiving Viread (Tenofovir Disoproxil)
Reported by a physician from Japan on 2007-10-22
Patient: male
Adverse reactions / side effects: Immune Reconstitution Syndrome, Cytomegalovirus Chorioretinitis, Bone Marrow Failure
Suspect drug(s):
Emtriva
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Start date: 2006-01-01
Viread
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Start date: 2006-01-01
Truvada
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Start date: 2005-12-10
End date: 2006-01-01
Other drugs received by patient: Efavirenz
Adverse event in 50 year old male receiving Viread (Tenofovir Disoproxil)
Reported by a health professional (non-physician/pharmacist) from France on 2007-10-22
Patient: 50 year old male
Adverse reactions / side effects: Blood Folate Decreased, Back Pain, Pain in Extremity, Fanconi Syndrome Acquired, Muscular Weakness, Extrapyramidal Disorder, Osteomalacia, Nerve Conduction Studies Abnormal
Adverse event resulted in: hospitalization
Suspect drug(s):
Viread (Tenofovir Disoproxil)
Other drugs received by patient: Epivir; Viracept; Depakine 500
Adverse event in 71 year old male receiving Viread (Tenofovir Disoproxil)
Reported by a health professional (non-physician/pharmacist) from France on 2007-10-22
Patient: 71 year old male, weighing 53.0 kg (116.6 pounds)
Adverse reactions / side effects: Neuropathy, Renal Tubular Disorder, Vitamin D Deficiency, Blood Parathyroid Hormone Increased
Suspect drug(s):
Sustiva
Start date: 2002-03-01
Zerit
Videx
Kaletra
Start date: 2002-03-01
Viread
Start date: 2002-03-01
Plaquenil
Other drugs received by patient: Virlix; Tenormin; Corvasal; Aspegic 325; Omeprazole
Adverse event in male receiving Viread (Tenofovir Disoproxil)
Reported by a health professional (non-physician/pharmacist) from France on 2007-10-22
Patient: male, weighing 53.0 kg (116.6 pounds)
Adverse reactions / side effects: Hypophosphataemia, Vitamin D Deficiency, Bone Pain, Pain
Adverse event resulted in: hospitalization
Suspect drug(s):
Viread
Administration route: Oral
Indication: HIV Infection
Start date: 2002-03-01
Kaletra
Administration route: Oral
Indication: HIV Infection
Start date: 2002-03-01
Sustiva
Administration route: Oral
Indication: HIV Infection
Start date: 2002-03-01
Plaquenil
Other drugs received by patient: Virlix; Tenormin; Corvasal; Aspegic 325
Adverse event in 24 year old male receiving Viread (Tenofovir Disoproxil)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-19
Patient: 24 year old male
Adverse reactions / side effects: Abdominal Pain, Weight Decreased, Hepatomegaly, Lymphadenopathy, Bacterial Infection, Gastritis, Ileus Paralytic
Suspect drug(s):
Reyataz
Administration route: Oral
Videx
Etibi
Lamivudine
Kaletra
Viread
Zithromax
Bactrim
Adverse event in 24 year old male receiving Viread (Tenofovir Disoproxil)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-18
Patient: 24 year old male
Adverse reactions / side effects: Abdominal Pain, Weight Decreased, Hepatomegaly, Lymphadenopathy, Bacterial Infection, Gastritis, Ileus Paralytic
Suspect drug(s):
Zithromax
Dosage: daily dose:600mg-freq:frequency: qd
Etibi
Dosage: daily dose:800mg-freq:frequency: qd
Kaletra
Dosage: text:3 df-freq:frequency: bid
Reyataz
Dosage: daily dose:300mg-freq:frequency: qd
Administration route: Oral
Lamivudine
Dosage: daily dose:150mg-freq:frequency: bid
Viread
Dosage: daily dose:300mg-freq:frequency: qd
Bactrim
Dosage: text:1 df-freq:frequency: qd
Videx
Dosage: daily dose:250mg-freq:frequency: qd
Adverse event in male receiving Viread (Tenofovir Disoproxil)
Reported by a health professional (non-physician/pharmacist) from France on 2007-10-16
Patient: male, weighing 53.0 kg (116.6 pounds)
Adverse reactions / side effects: Hypophosphataemia, Vitamin D Deficiency, Pain in Extremity, Pain
Adverse event resulted in: hospitalization
Suspect drug(s):
Sustiva
Administration route: Oral
Indication: HIV Infection
Start date: 2002-03-01
Kaletra
Administration route: Oral
Indication: HIV Infection
Start date: 2002-03-01
Viread
Administration route: Oral
Indication: HIV Infection
Start date: 2002-03-01
Plaquenil
Dosage: unk
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Other drugs received by patient: Aspegic 325; Corvasal; Tenormin; Virlix; Omeprazole
Adverse event in 43 year old male receiving Viread (Tenofovir Disoproxil)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-16
Patient: 43 year old male
Adverse reactions / side effects: Immune Reconstitution Syndrome, Cytomegalovirus Chorioretinitis, Bone Marrow Failure
Adverse event resulted in: hospitalization
Suspect drug(s):
Stocrin Caps
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Start date: 2005-12-10
Baktar
Administration route: Oral
Indication: Pneumocystis Jiroveci Pneumonia
Start date: 2006-01-01
Viread
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Start date: 2006-01-01
Emtriva
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Start date: 2006-01-01
Valixa
Administration route: Oral
Indication: Cytomegalovirus Chorioretinitis
Start date: 2006-01-17
Truvada
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Start date: 2005-12-10
End date: 2006-01-01
Rabeprazole Sodium
Administration route: Oral
Indication: Adverse Drug Reaction
Start date: 2005-12-01
Gasmotin
Administration route: Oral
Indication: Adverse Drug Reaction
Start date: 2006-01-01
Adverse event in 24 year old male receiving Viread (Tenofovir Disoproxil)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-15
Patient: 24 year old male
Adverse reactions / side effects: Abdominal Pain, Weight Decreased, Gastrointestinal Motility Disorder, Hepatomegaly, Vomiting, Nausea, Gastritis
Suspect drug(s):
Zithromax
Dosage: daily dose:600mg
Etibi
Dosage: daily dose:800mg
Reyataz
Dosage: daily dose:300mg
Videx
Dosage: daily dose:250mg
Lamivudine
Viread
Kaletra
Bactrim
Adverse event in 52 year old male receiving Viread (Tenofovir Disoproxil)
Reported by a physician from France on 2007-10-15
Patient: 52 year old male
Adverse reactions / side effects: Optic Neuritis Retrobulbar
Adverse event resulted in: disablity
Suspect drug(s):
Invirase
Dosage: reported dosing amount: 4 doses daily.
Start date: 2006-06-23
Invirase
Start date: 2002-03-18
Bactrim DS
Dosage: also received on 28 september 2005 and 23 june 2006.
Indication: Drug USE FOR Unknown Indication
Start date: 1998-10-27
Combivir
Dosage: reported dosing amount: 2 doses daily.
Start date: 2005-09-28
End date: 2006-06-23
Combivir
Start date: 1999-05-11
End date: 1999-08-01
Combivir
Start date: 2001-03-23
Telzir
Dosage: reported dosing amount: 2 doses daily. also received on 17 june 2005.
Start date: 2005-03-29
End date: 2006-06-23
Norvir
Dosage: also received on 15 october 2004, 29 march 2005, 28 september 2005, 17 june 2005 and 23 june 2006.
Start date: 2004-04-17
Norvir
Start date: 1999-09-21
Norvir
Start date: 2000-06-06
Norvir
Start date: 2001-03-23
Norvir
Start date: 2002-03-18
Neurontin
Indication: Trigeminal Neuralgia
Start date: 2006-01-01
Lyrica
Indication: Trigeminal Neuralgia
Start date: 2006-06-23
Retrovir
Indication: Drug USE FOR Unknown Indication
Start date: 2006-06-23
Retrovir
Start date: 2005-06-17
Viread
Indication: Drug USE FOR Unknown Indication
Start date: 2006-06-23
Viread
Start date: 2003-01-03
Viread
Start date: 2003-09-12
Viread
Start date: 2004-04-17
Viread
Start date: 2004-10-15
Viread
Start date: 2005-03-29
Viread
Start date: 2005-06-17
Other drugs received by patient: Sustiva; Videx; Videx; Videx; Zerit; Zerit; Zerit; Zerit; Hivid; Hivid; Crixivan; Crixivan; 1 Concomitant Drug; Epivir; Agenerase; Kaletra; Kaletra; Fuzeon; Fuzeon; 1 Concomitant Drug; 1 Concomitant Drug; Ziagen; Tercian; Laroxyl; Tenofovir
Adverse event in male receiving Viread (Tenofovir Disoproxil)
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-10-15
Patient: male
Adverse reactions / side effects: Abdominal Hernia, Cardiac Murmur, Cryptorchism, Abdominal Distension
Suspect drug(s):
Viread
Indication: HIV Infection
Start date: 2004-06-01
End date: 2004-07-20
Combivir
Indication: HIV Infection
Start date: 2004-01-30
End date: 2004-06-01
Viracept
Indication: HIV Infection
Start date: 2004-01-30
End date: 2004-07-20
Kaletra
Indication: HIV Infection
Start date: 2004-06-01
Retrovir
Indication: HIV Infection
Start date: 2004-06-01
End date: 2004-07-20
Other drugs received by patient: Folic Acid
Adverse event in female receiving Viread (Tenofovir Disoproxil)
Reported by a physician from United States on 2007-10-15
Patient: female, weighing 20.0 kg (44.0 pounds)
Adverse reactions / side effects: Weight Decreased, Fanconi Syndrome, Hyperglycaemia, Nephrogenic Diabetes Insipidus
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Viread
Administration route: Oral
Indication: HIV Infection
Start date: 2005-01-01
End date: 2007-09-12
Kaletra
Administration route: Oral
Indication: HIV Infection
Start date: 2005-01-01
End date: 2007-09-12
DDI
Administration route: Oral
Indication: HIV Infection
Start date: 2005-01-01
End date: 2007-09-12
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