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This is an index of reports of adverse events (side effects, adverse reactions, etc.) related to Sustiva (Efavirenz). 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 (126)
Cases resulting in a serious event (126)
Cases resulting in death (14)
Cases resulting in life threatening events (8)
Cases resulting in hospitalization (57)
Cases resulting in disability (14)
Cases resulting in other serious reactions (69)
Below is a sample of reports where side effects / adverse reactions may be related to Sustiva (Efavirenz). For a complete list and/or a specific selection of reports, please use the links in the index above.
Adverse event in male receiving Sustiva (Efavirenz)
Reported by a physician from United States on 2007-10-31
Patient: male
Adverse reactions / side effects: Pregnancy, Hypospadias, Chordee
Suspect drug(s):
Blinded: Indinavir
Indication: HIV Infection
Didanosine
Dosage: exposure during 1, 2, 3 trimester
Indication: HIV Infection
Lamivudine
Dosage: exposure during 1st through 3rd trimester
Indication: HIV Infection
Nelfinavir
Dosage: exposure during 1st through 3rd trimester
Administration route: Oral
Indication: HIV Infection
Ritonavir
Dosage: exposure during 3rd trimester
Indication: HIV Infection
Sustiva
Dosage: exposure during 3rd trimester
Indication: HIV Infection
Zidovudine
Dosage: exposure during 1st through 3rd trimester
Indication: HIV Infection
Adverse event in female receiving Sustiva (Efavirenz)
Reported by a individual with unspecified qualification from France on 2007-10-31
Patient: female, weighing 54.0 kg (118.8 pounds)
Adverse reactions / side effects: Abdominal Pain, Weight Decreased, Vomiting, Anorexia, Pyrexia, Asthenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Sustiva
Administration route: Oral
Indication: HIV Infection
Start date: 2007-09-18
Truvada
Administration route: Oral
Indication: HIV Infection
Start date: 2007-09-18
Other drugs received by patient: Rifadin; Rimifon; Bactrim LOW; Lederfoline; Zelitrex; Tardiferon; Stilnox
Adverse event in 29 year old female receiving Sustiva (Efavirenz)
Reported by a health professional (non-physician/pharmacist) from France on 2007-10-26
Patient: 29 year old female, weighing 54.0 kg (118.8 pounds)
Adverse reactions / side effects: Viral Infection
Adverse event resulted in: hospitalization
Suspect drug(s):
Sustiva
Indication: HIV Infection
Start date: 2007-09-18
Truvada
Dosage: 1 dosage form-1 tablet
Indication: HIV Infection
Start date: 2007-09-18
Other drugs received by patient: Rifadin; Rimifon; Bactrim; Lederfoline; Zelitrex; Tardyferon
Adverse event in 40 year old male receiving Sustiva (Efavirenz)
Reported by a consumer/non-health professional from Italy on 2007-10-24
Patient: 40 year old male
Adverse reactions / side effects: Thrombocytopenia
Suspect drug(s):
Sustiva (Efavirenz)
Other drugs received by patient: Truvada
Adverse event in female receiving Sustiva (Efavirenz)
Reported by a consumer/non-health professional from United States on 2007-10-24
Patient: female
Adverse reactions / side effects: Type 2 Diabetes Mellitus
Suspect drug(s):
Combivir
Dosage: patient received combivir tablet for a period of 8 years.
Sustiva
Adverse event in male receiving Sustiva (Efavirenz)
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):
Kaletra
Administration route: Oral
Indication: HIV Infection
Start date: 2002-03-01
Plaquenil
Sustiva
Administration route: Oral
Indication: HIV Infection
Start date: 2002-03-01
Viread
Administration route: Oral
Indication: HIV Infection
Start date: 2002-03-01
Other drugs received by patient: Virlix; Tenormin; Corvasal; Aspegic 325
Adverse event in 71 year old male receiving Sustiva (Efavirenz)
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):
Kaletra
Start date: 2002-03-01
Plaquenil
Sustiva
Start date: 2002-03-01
Videx
Viread
Start date: 2002-03-01
Zerit
Other drugs received by patient: Virlix; Tenormin; Corvasal; Aspegic 325; Omeprazole
Adverse event in receiving Sustiva (Efavirenz)
Reported by a individual with unspecified qualification from United States on 2007-10-19
Patient:
Adverse reactions / side effects: Drug Exposure During Pregnancy, Hypospadias
Suspect drug(s):
Epivir
Indinivir Sulfate
Norvir
Retrovir
Sustiva
Videx
Viracept
Administration route: Oral
Indication: HIV Infection
Adverse event in female receiving Sustiva (Efavirenz)
Reported by a individual with unspecified qualification from France on 2007-10-19
Patient: female, weighing 54.0 kg (118.8 pounds)
Adverse reactions / side effects: Abdominal Pain, Weight Decreased, Vomiting, Anorexia, Pyrexia, Asthenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Sustiva
Administration route: Oral
Indication: HIV Infection
Start date: 2007-09-18
Truvada
Administration route: Oral
Indication: HIV Infection
Start date: 2007-09-18
Other drugs received by patient: Rifadin; Rimifon; Rifinah; Bactrim LOW; Lederfoline; Zelitrex; Tardiferon
Adverse event in male receiving Sustiva (Efavirenz)
Reported by a individual with unspecified qualification from France on 2007-10-18
Patient: male, weighing 83.0 kg (182.6 pounds)
Adverse reactions / side effects: Jaundice, Anorexia
Suspect drug(s):
Bactrim
Administration route: Oral
Start date: 2007-06-13
End date: 2007-09-21
Rifampicin
Administration route: Oral
Indication: Tuberculosis
Start date: 2007-07-13
End date: 2007-09-21
Rifinah
Administration route: Oral
Indication: Tuberculosis
Start date: 2007-07-13
End date: 2007-09-21
Sustiva
Administration route: Oral
Indication: HIV Infection
Start date: 2007-08-22
End date: 2007-09-21
Truvada
Administration route: Oral
Indication: HIV Infection
Start date: 2007-08-22
Adverse event in male receiving Sustiva (Efavirenz)
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):
Kaletra
Administration route: Oral
Indication: HIV Infection
Start date: 2002-03-01
Plaquenil
Dosage: unk
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Sustiva
Administration route: Oral
Indication: HIV Infection
Start date: 2002-03-01
Viread
Administration route: Oral
Indication: HIV Infection
Start date: 2002-03-01
Other drugs received by patient: Aspegic 325; Corvasal; Tenormin; Virlix; Omeprazole
Adverse event in 31 year old female receiving Sustiva (Efavirenz)
Reported by a physician from Germany on 2007-10-15
Patient: 31 year old female
Adverse reactions / side effects: Stress, Abortion Spontaneous, Pregnancy
Suspect drug(s):
Sustiva (Efavirenz)
Other drugs received by patient: Truvada
Adverse event in 53 year old male receiving Sustiva (Efavirenz)
Reported by a physician from United States on 2007-10-12
Patient: 53 year old male
Adverse reactions / side effects: Aspartate Aminotransferase Increased, Alanine Aminotransferase Increased
Suspect drug(s):
Epivir
Dosage: 300mg per day
Administration route: Oral
Indication: HIV Infection
Letairis
Dosage: 5mg per day
Administration route: Oral
Start date: 2007-08-09
End date: 2007-09-12
Spiriva
Sustiva
Dosage: 600mg per day
Administration route: Oral
Indication: HIV Infection
Viread
Dosage: 300mg per day
Indication: HIV Infection
Other drugs received by patient: Lasix; Sildenafil Citrate; Warfarin Sodium; Advair Diskus 100 / 50; Singulair; Metformin HCL; Flomax; Wellbutrin
Adverse event in female receiving Sustiva (Efavirenz)
Reported by a consumer/non-health professional from United States on 2007-10-09
Patient: female
Adverse reactions / side effects: Type 2 Diabetes Mellitus
Suspect drug(s):
Combivir
Indication: Drug USE FOR Unknown Indication
Sustiva
Indication: Drug USE FOR Unknown Indication
Adverse event in 45 year old male receiving Sustiva (Efavirenz)
Reported by a physician from France on 2007-10-09
Patient: 45 year old male
Adverse reactions / side effects: Hypovitaminosis
Adverse event resulted in: hospitalization
Suspect drug(s):
Epivir
Sustiva
Tenofovir
Adverse event in female receiving Sustiva (Efavirenz)
Reported by a consumer/non-health professional from United States on 2007-10-09
Patient: female
Adverse reactions / side effects: Type 2 Diabetes Mellitus
Suspect drug(s):
Combivir
Indication: Drug USE FOR Unknown Indication
Sustiva
Indication: Drug USE FOR Unknown Indication
Adverse event in 45 year old male receiving Sustiva (Efavirenz)
Reported by a physician from France on 2007-10-09
Patient: 45 year old male
Adverse reactions / side effects: Hypovitaminosis
Adverse event resulted in: hospitalization
Suspect drug(s):
Epivir
Sustiva
Tenofovir
Adverse event in 471 month old female receiving Sustiva (Efavirenz)
Reported by a health professional (non-physician/pharmacist) from France on 2007-10-03
Patient: 471 month old female
Adverse reactions / side effects: Hepatitis Fulminant
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Hytacand
Administration route: Oral
Indication: Hypertension
Start date: 2007-02-01
End date: 2007-06-13
Rulid
Administration route: Oral
Indication: Chlamydial Infection
Start date: 2007-05-01
End date: 2007-05-15
Sustiva
Administration route: Oral
Indication: HIV Infection
Start date: 2007-01-01
End date: 2007-06-13
Truvada
Dosage: 200 + 245 mg daily
Administration route: Oral
Indication: HIV Infection
Start date: 2007-01-01
End date: 2007-06-13
Other drugs received by patient: Inipomp; Bactrim
Adverse event in female receiving Sustiva (Efavirenz)
Reported by a health professional (non-physician/pharmacist) from France on 2007-10-02
Patient: female
Adverse reactions / side effects: Brain Death, Hepatic Encephalopathy, Hepatitis Fulminant
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Hytacand
Indication: Hypertension
Start date: 2007-02-01
End date: 2007-06-13
Rulid
Indication: Chlamydial Infection
Start date: 2007-05-01
End date: 2007-05-15
Sustiva
Administration route: Oral
Indication: HIV Infection
Start date: 2007-01-01
End date: 2007-06-13
Truvada
Administration route: Oral
Indication: HIV Infection
Start date: 2007-01-01
End date: 2007-06-13
Other drugs received by patient: Inipomp; Bactrim
Adverse event in male receiving Sustiva (Efavirenz)
Reported by a individual with unspecified qualification from France on 2007-10-02
Patient: male, weighing 60.0 kg (132.0 pounds)
Adverse reactions / side effects: Lymphadenitis, Immune Reconstitution Syndrome, Vomiting, Pyrexia, Cryptococcosis
Adverse event resulted in: hospitalization
Suspect drug(s):
Sustiva
Administration route: Oral
Indication: HIV Infection
Start date: 2006-08-31
Truvada
Administration route: Oral
Indication: HIV Infection
Start date: 2006-08-31
Other drugs received by patient: Cortancyl; Triflucan; Bactrim; Myambutol; Zeclar; Rifater; Zelitrex; Hydrocortisone; Rifinah
Adverse event in 33 year old male receiving Sustiva (Efavirenz)
Reported by a consumer/non-health professional from France on 2007-10-02
Patient: 33 year old male
Adverse reactions / side effects: Dyspnoea, Haemoptysis, Chest Pain, Suicide Attempt, Pulmonary Embolism, Pulmonary Infarction
Adverse event resulted in: hospitalization
Suspect drug(s):
Combivir
Dosage: 2tab per day
Administration route: Oral
Indication: HIV Infection
Start date: 2001-10-15
Norset
Dosage: 2tab per day
Administration route: Oral
Indication: Depression
Sustiva
Dosage: 2tab per day
Administration route: Oral
Indication: HIV Infection
Start date: 2003-03-15
Adverse event in male receiving Sustiva (Efavirenz)
Reported by a health professional (non-physician/pharmacist) from France on 2007-10-01
Patient: male, weighing 61.0 kg (134.2 pounds)
Adverse reactions / side effects: Psychotic Disorder, Pyrexia, Tuberculoma of Central Nervous System, Convulsion
Adverse event resulted in: hospitalization
Suspect drug(s):
Bactrim
Indication: Pneumocystis Jiroveci Pneumonia
Start date: 2005-11-26
Dexambutol
Indication: Tuberculosis
Start date: 2005-12-05
Rifater
Indication: Tuberculosis
Start date: 2005-11-30
Sustiva
Administration route: Oral
Indication: HIV Infection
Start date: 2006-01-05
End date: 2006-01-13
Other drugs received by patient: Truvada
Adverse event in 34 year old male receiving Sustiva (Efavirenz)
Reported by a health professional (non-physician/pharmacist) from France on 2007-10-01
Patient: 34 year old male
Adverse reactions / side effects: Pulmonary Embolism
Adverse event resulted in: hospitalization
Suspect drug(s):
Combivir
Start date: 2001-10-15
Norset
Sustiva
Start date: 2003-03-15
Adverse event in 39 year old male receiving Sustiva (Efavirenz)
Reported by a health professional (non-physician/pharmacist) from France on 2007-07-31
Patient: 39 year old male, weighing 76.0 kg (167.2 pounds)
Adverse reactions / side effects: Brain Stem Syndrome, Nervous System Disorder, Intracranial Pressure Increased, Inflammation
Adverse event resulted in: hospitalization
Suspect drug(s):
Amiklin INJ
Indication: Tuberculosis
Start date: 2007-05-07
Izilox
Indication: Tuberculosis
Start date: 2007-05-07
Myambutol
Indication: Tuberculosis
Start date: 2007-05-07
Pirilene
Indication: Tuberculosis
Start date: 2007-05-14
Rimifon
Indication: Tuberculosis
Start date: 2007-05-14
Sustiva
Administration route: Oral
Indication: HIV Infection
Start date: 2007-06-01
Truvada
Indication: HIV Infection
Start date: 2007-06-01
Other drugs received by patient: Bactrim; Depakene; Azadose
Adverse event in male receiving Sustiva (Efavirenz)
Reported by a physician from France on 2007-07-30
Patient: male, weighing 72.0 kg (158.4 pounds)
Adverse reactions / side effects: Rhabdomyolysis
Suspect drug(s):
Kaletra
Administration route: Oral
Indication: HIV Infection
Start date: 2007-05-03
End date: 2007-05-16
Sustiva
Start date: 2007-06-07
Truvada
Administration route: Oral
Indication: HIV Infection
Start date: 2007-05-03
End date: 2007-05-16
Truvada
Start date: 2007-06-07
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