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Index of reports
> Cases resulting in life threatening events (9)
Below is the selection of adverse event reports related to Zithromax (Azithromycin) that includes cases resulting in life threatening events.
Adverse event in 46 year old female receiving Zithromax (Azithromycin)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-09
Patient: 46 year old female, weighing 81.6 kg (179.6 pounds)
Adverse reactions / side effects: Malaise, Therapeutic Response Unexpected With Drug Substitution, Pharmaceutical Product Counterfeit, Pharmaceutical Product Complaint
Adverse event resulted in: life threatening event
Suspect drug(s):
Zithromax
Dosage: 6 tabs one daily po
Administration route: Oral
Indication: Ear Infection
Start date: 2007-10-08
End date: 2007-10-08
Zithromax
Dosage: 6 tabs one daily po
Administration route: Oral
Indication: Pharyngitis
Start date: 2007-10-08
End date: 2007-10-08
Adverse event in 36 year old male receiving Zithromax (Azithromycin)
Reported by a physician from Japan on 2007-10-01
Patient: 36 year old male
Adverse reactions / side effects: Blood Urea Increased, AIDS Encephalopathy, Altered State of Consciousness, Blood Creatinine Increased, Renal Failure Chronic, Convulsion, Nephropathy
Adverse event resulted in: life threatening event
Suspect drug(s):
Ziagen
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Start date: 2002-11-26
End date: 2007-03-17
Viread
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Start date: 2003-05-20
End date: 2006-11-14
Epivir
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Start date: 2000-09-19
End date: 2007-03-17
Retrovir
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Start date: 2000-09-19
End date: 2006-12-11
Norvir
Dosage: 100mg as directed
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Start date: 2004-04-07
End date: 2007-03-17
Norvir
Dosage: 200mg unknown
Administration route: Oral
Indication: Acquired Immunodeficiency Syndrome
Start date: 2003-05-20
End date: 2003-11-10
Zithromax
Administration route: Oral
Indication: Opportunistic Infection Prophylaxis
Start date: 2002-04-09
Baktar
Administration route: Oral
Indication: Antifungal Prophylaxis
Start date: 2006-04-01
Tipranavir
Indication: Drug USE FOR Unknown Indication
Darunavir
Indication: Drug USE FOR Unknown Indication
Other drugs received by patient: Unknown Drug; Unknown Drug
Adverse event in male receiving Zithromax (Azithromycin)
Reported by a consumer/non-health professional from United States on 2007-07-18
Patient: male, weighing 94.3 kg (207.5 pounds)
Adverse reactions / side effects: Endocarditis Bacterial, Body Temperature Increased, Drug Ineffective, Chills, Pain, Cerebrovascular Accident, Syncope, Malaise, Oedema Peripheral, Pigmentation Disorder, Skin Lesion, Feeling Abnormal
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Zithromax
Administration route: Oral
Indication: Influenza Like Illness
Start date: 2003-10-08
End date: 2003-10-11
Zithromax
Indication: Pharyngitis
Other drugs received by patient: Glucophage; Glyburide
Adverse event in 36 year old male receiving Zithromax (Azithromycin)
Reported by a physician from United States on 2007-06-08
Patient: 36 year old male
Adverse reactions / side effects: LIP Swelling, Oral Mucosal Blistering, Rash Pruritic, Oedema Peripheral, Blindness, Conjunctival Scar, Pharyngitis, Stevens-Johnson Syndrome
Adverse event resulted in: life threatening event, hospitalization, disablity
Suspect drug(s):
Zithromax
Lamictal
Administration route: Oral
Indication: Bipolar Disorder
Start date: 2006-10-23
End date: 2006-11-21
Omnicef
Indication: Pharyngitis
Medrol
Vicodin
Other drugs received by patient: Sertraline Hydrochloride; Mometasone Furoate; Sumatriptan Succinate; Hydrochlorothiazide
Adverse event in 3 year old male receiving Zithromax (Azithromycin)
Reported by a pharmacist from Spain on 2007-04-09
Patient: 3 year old male, weighing 14.0 kg (30.8 pounds)
Adverse reactions / side effects: Thrombocytopenic Purpura
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Zithromax (Azithromycin)
Adverse event in female receiving Zithromax (Azithromycin)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-04-09
Patient: female
Adverse reactions / side effects: NO Adverse Effect
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Zithromax
Indication: Sinusitis
Domperidone
Administration route: Oral
Indication: Lactation Disorder
Adverse event in male receiving Zithromax (Azithromycin)
Reported by a consumer/non-health professional from Denmark on 2007-04-06
Patient: male, weighing 83.0 kg (182.6 pounds)
Adverse reactions / side effects: Palpitations, Angina Pectoris, Heart Rate Increased, Atrial Fibrillation, Heart Rate Irregular, Hypertension
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Zithromax (Azithromycin)
Adverse event in male receiving Zithromax (Azithromycin)
Reported by a individual with unspecified qualification from United States on 2007-02-16
Patient: male, weighing 74.8 kg (164.7 pounds)
Adverse reactions / side effects: Autoimmune Hepatitis
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Zithromax (Azithromycin)
Adverse event in male receiving Zithromax (Azithromycin)
Reported by a physician from Netherlands on 2007-01-19
Patient: male
Adverse reactions / side effects: Myocardial Infarction
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Zithromax (Azithromycin)
Other drugs received by patient possibly interacting with the suspect drug:
Neoral
Start date: 2006-01-01
Other drugs received by patient: Depakene; Lormetazepam
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