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Fluconazole (Fluconazole) - Reports of Side Effects & Adverse Reactions

 



This is an index of reports of adverse events (side effects, adverse reactions, etc.) related to Fluconazole. 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 (129)
     Toxic Epidermal Necrolysis (19)Drug Interaction (13)Rhabdomyolysis (12)more >>

Cases resulting in a serious event (123)
     Toxic Epidermal Necrolysis (19)Drug Interaction (13)Rhabdomyolysis (12)more >>

Cases resulting in death (13)
     Leukopenia (3)Bronchopulmonary Aspergillosis (2)Venous Haemorrhage (2)more >>

Cases resulting in life threatening events (19)
     Toxic Epidermal Necrolysis (5)Fall (5)Leukopenia (5)more >>

Cases resulting in hospitalization (56)
     Renal Impairment (12)Rhabdomyolysis (10)Renal Failure Acute (10)more >>

Cases resulting in disability (10)
     Renal Failure (6)Neuropathy Peripheral (4)Purpura Senile (4)more >>

Cases resulting in other serious reactions (64)
     Toxic Epidermal Necrolysis (15)Rash (6)Nausea (5)more >>

Below is a sample of reports where side effects / adverse reactions may be related to Fluconazole. For a complete list and/or a specific selection of reports, please use the links in the index above.

Adverse event in 21 year old male receiving Fluconazole

Reported by a pharmacist from United States on 2007-10-31

Patient: 21 year old male, weighing 30.0 kg (66.0 pounds)

Adverse reactions / side effects: Pancreatitis

Adverse event resulted in: hospitalization

Suspect drug(s):
Ativan
    Indication: Agitation
    Start date: 2007-07-01

Clonidine
    Administration route: Topical
    Indication: Neuralgia
    Start date: 2007-07-24
    End date: 2007-08-03

Demerol
    Dosage: 25 to 50 mg every two hours
    Indication: Pain
    Start date: 2007-07-30
    End date: 2007-08-03

Diazepam
    Indication: Agitation
    Start date: 2007-07-01

Fluconazole
    Indication: Candidiasis
    Start date: 2007-07-29
    End date: 2007-08-03

Keppra
    Indication: Convulsion
    Start date: 2007-07-12
    End date: 2007-08-03

Methadone HCL
    Administration route: Oral
    Indication: Drug Withdrawal Syndrome
    Start date: 2007-07-29
    End date: 2007-08-03

Methadone HCL
    Administration route: Oral
    Indication: Pain
    Start date: 2007-07-29
    End date: 2007-08-03

Nexium
    Indication: Reflux Oesophagitis
    Start date: 2007-07-29
    End date: 2007-08-13

Paxil
    Administration route: Oral
    Indication: Depression
    Start date: 2007-07-25
    End date: 2007-08-03

Pepcid
    Start date: 2007-07-01

Other drugs received by patient: Chloral Hydrate; Unasyn; Bisacodyl; Diazepam; Dexmedetomidine; Ketamine HCL



Adverse event in 63 year old female receiving Fluconazole

Reported by a health professional (non-physician/pharmacist) from Portugal on 2007-10-30

Patient: 63 year old female

Adverse reactions / side effects: Drug Interaction, Toxic Skin Eruption

Adverse event resulted in: disablity

Suspect drug(s):
Fluconazole
    Dosage: oral
    Administration route: Oral
    Indication: Mucosal Inflammation
    Start date: 2007-04-26

Paclitaxel
    Dosage: 270 mg, 1 in 3 wk), intravenous
    Indication: Ovarian Epithelial Cancer
    Start date: 2007-04-26
    End date: 2007-07-24

Other drugs received by patient: Carboplatin; Dicyclomine HCL; Metoclopramide; Doxylamine; Pyridoxine; Dosulepin



Adverse event in receiving Fluconazole

Reported by a physician from United States on 2007-10-30

Patient:

Adverse reactions / side effects: Hypokalaemia

Adverse event resulted in: hospitalization

Suspect drug(s):
Augmentin '125'
    Dosage: 1 mg, 3 in qd
    Indication: Drug USE FOR Unknown Indication
    Start date: 2007-06-27
    End date: 2007-07-02

Fluconazole
    Dosage: unk
    Indication: Drug USE FOR Unknown Indication
    Start date: 2007-06-30
    End date: 2007-07-05

Inipomp
    Dosage: unk
    Indication: Drug USE FOR Unknown Indication
    Start date: 2007-06-27

Metoclopramide
    Dosage: 10 mg in 2 ml, qd
    Indication: Drug USE FOR Unknown Indication
    Start date: 2007-06-27
    End date: 2007-07-02

Tamsulosin HCL
    Dosage: 0.4 mg, unk
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication
    Start date: 2007-06-28
    End date: 2007-07-03

Verapamil
    Dosage: 3 g, unk
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication
    Start date: 2007-06-27
    End date: 2007-07-03



Adverse event in 54 year old male receiving Fluconazole

Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-30

Patient: 54 year old male

Adverse reactions / side effects: Pulmonary Embolism

Adverse event resulted in: hospitalization

Suspect drug(s):
Fluconazole
    Dosage: 200 mg
    Indication: Pneumonia Cryptococcal
    Start date: 2007-03-29

Mycophenolate Mofetil
    Dosage: 500 mg, bid, oral
    Administration route: Oral
    Indication: Liver Transplant
    Start date: 2006-11-08

Prednisone
    Dosage: 2.5 mg, uid/qd, oral
    Administration route: Oral
    Indication: Liver Transplant
    Start date: 2006-09-13

Prograf
    Dosage: 0.5 mg, bid, oral
    Administration route: Oral
    Indication: Liver Transplant
    Start date: 2006-09-13

Other drugs received by patient: Protonix; Actigall; Magnesium Oxide (Magnesium Oxide); Calcium with Vitamin D (Ergocalciferol, Calcium Sodium Lactate, Calciu; Actonel



Adverse event in male receiving Fluconazole

Reported by a pharmacist from United States on 2007-10-30

Patient: male, weighing 33.4 kg (73.5 pounds)

Adverse reactions / side effects: Blood Amylase Increased, Pancreatitis, Lipase Increased

Adverse event resulted in: hospitalization

Suspect drug(s):
Ativan
    Dosage: text:3-4.5mg-freq:q3-4h: prn
    Indication: Agitation
    Start date: 2007-07-06
    End date: 2007-08-03

Clonidine
    Indication: Neuralgia

Demerol
    Dosage: text:25-50 mg-freq:q2h: prn
    Indication: Pain
    Start date: 2007-07-30
    End date: 2007-08-03

Diazepam
    Indication: Agitation

Fluconazole
    Indication: Systemic Candida
    Start date: 2007-07-29
    End date: 2007-08-03

Keppra
    Indication: Convulsion
    Start date: 2007-07-12
    End date: 2007-08-03

Methadone HCL
    Administration route: Oral
    Indication: Pain
    Start date: 2007-07-29
    End date: 2007-08-03

Methadone HCL
    Indication: Sedation

Nexium
    Indication: Gastrooesophageal Reflux Disease
    Start date: 2007-07-29
    End date: 2007-08-03

Paxil
    Dosage: daily dose:15mg
    Administration route: Oral
    Start date: 2007-07-01
    End date: 2007-08-03



Adverse event in female receiving Fluconazole

Reported by a individual with unspecified qualification on 2007-10-29

Patient: female

Adverse reactions / side effects: Abdominal Abscess, Peritonitis, Disease Progression

Adverse event resulted in: death

Suspect drug(s):
Fluconazole
    Administration route: Oral
    Indication: Coccidioidomycosis

Interferon Gamma
    Indication: Coccidioidomycosis

Voriconazole
    Indication: Coccidioidomycosis



Adverse event in 11 year old male receiving Fluconazole

Reported by a health professional (non-physician/pharmacist) from Canada on 2007-10-29

Patient: 11 year old male

Adverse reactions / side effects: Torsade DE Pointes, Ventricular Extrasystoles, Respiratory Acidosis, Ventricular Tachycardia, Hypomagnesaemia, Pulse Absent, Drug Interaction

Adverse event resulted in: life threatening event

Suspect drug(s):
Amiodarone HCL
    Dosage: 5 mg/kg, intravenous

Fluconazole
    Dosage: 150 mg, q12h, intravenous
    Indication: Candidiasis

Furosemide

Other drugs received by patient: Meropenem (Meropenem); Midazolam HCL; Lorazepam; Chloral Hydrate (Chloral Hydrate); Acetaminophen; Ibuprofen



Adverse event in 36 year old male receiving Fluconazole

Reported by a physician from Italy on 2007-10-25

Patient: 36 year old male

Adverse reactions / side effects: Application Site Reaction, Blood Bilirubin Increased, Pruritus, Skin Exfoliation, Hyperpyrexia, Hypokalaemia, Bacterial Toxaemia, Gamma-Glutamyltransferase Increased, Hepatotoxicity, Electrolyte Imbalance, Nephropathy Toxic, Alanine Aminotransferase Increased, Anaemia, Febrile Neutropenia, Blood Fibrinogen Increased, Agranulocytosis, Sepsis, Aspartate Aminotransferase Increased, Rash Maculo-Papular, Leukocytosis, Leukopenia, Infusion Site Reaction

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Amikacin
    Dosage: 1000 mg, qd, intravenous
    Indication: Febrile Neutropenia

Amphotericin B
    Dosage: 3 mg/kg, qd, intravenous
    Indication: Febrile Neutropenia

Cefotaxime
    Indication: Evidence Based Treatment

Ciprofloxacin
    Indication: Evidence Based Treatment

Clozapine (Ngx)(clozapine) Unknown
    Indication: Depression

Fluconazole
    Dosage: 600 mg, qd, intravenous
    Indication: Febrile Neutropenia

Meropenem(meropenem)
    Dosage: 6 g, qd, intravenous
    Indication: Febrile Neutropenia

Neupogen
    Dosage: 5 ug/kg, qd, subcutaneous; 10 ug/kg, qd,
    Indication: Agranulocytosis

Teicoplanin(teicoplanin)
    Dosage: 800 mg, qd, intravenous; 600 mg, qd, intravenous
    Indication: Febrile Neutropenia

Other drugs received by patient: Lithium Carbonate; Citalopram (Citalopram); Clomipramine HCL; Lorazepam



Adverse event in 41 year old male receiving Fluconazole

Reported by a pharmacist from Spain on 2007-10-25

Patient: 41 year old male

Adverse reactions / side effects: Pancytopenia

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Fluconazole
    Dosage: daily dose:100mg
    Administration route: Oral
    Indication: Oral Candidiasis
    Start date: 2006-08-03
    End date: 2006-08-17

Septrin
    Administration route: Oral
    Indication: Pneumonia



Adverse event in male receiving Fluconazole

Reported by a consumer/non-health professional from United States on 2007-10-24

Patient: male

Adverse reactions / side effects: Intestinal Functional Disorder

Suspect drug(s):
Fluconazole



Adverse event in 56 year old male receiving Fluconazole

Reported by a individual with unspecified qualification from Italy on 2007-10-23

Patient: 56 year old male

Adverse reactions / side effects: Back Pain, Pneumonia, Coronary Artery Disease, Drug Interaction, Immunosuppressant Drug Level Increased, Self-Medication, Acute Myocardial Infarction, Leukopenia, Renal Failure Acute

Adverse event resulted in: hospitalization

Suspect drug(s):
Ciclosporin Microemulsion (Ciclosporin)
    Dosage: 250 mg; 200 mg; 150 mg; 75 mg
    Indication: Immunosuppressant Drug Therapy

Everolimus (Everolimus) (Everolimus)
    Dosage: 1.5 mg (twice daily)
    Indication: Angiopathy

Fluconazole
    Indication: Pneumonia

Other drugs received by patient: Ciprofloxacin; Nimesulide (Nimesulide) (Nimesulide)



Adverse event in 42 year old male receiving Fluconazole

Reported by a individual with unspecified qualification from Canada on 2007-10-23

Patient: 42 year old male

Adverse reactions / side effects: Pneumocystis Jiroveci Pneumonia, Anticoagulation Drug Level Below Therapeutic, Incorrect Drug Administration Duration, HIV Test Positive, International Normalised Ratio Decreased, Incorrect Dose Administered, International Normalised Ratio Increased, Drug Interaction, Depression, Treatment Noncompliance, Candidiasis

Suspect drug(s):
Fluconazole
    Dosage: qd
    Indication: Candidiasis

Warfarin Sodium
    Dosage: 5.5 mg; qd; 3 mg; qod; 3.5 mg; qod; 11 mg; qd
    Indication: Aortic Valve Replacement

Other drugs received by patient: Citalopram (Citalopram); Clonazepam; Zopiclone (Zopiclone); Pantoprazole Sodium; Sulfamethoxazole; Trimethoprim; Zidovudine; Lamivudine



Adverse event in female receiving Fluconazole

Reported by a physician from United States on 2007-10-22

Patient: female

Adverse reactions / side effects: Drug Toxicity, Liver Function Test Abnormal, Mucormycosis, Renal Failure Acute

Adverse event resulted in: hospitalization

Suspect drug(s):
Caspofungin Acetate
    Dosage: unspecified
    Indication: Bronchopulmonary Aspergillosis
    Start date: 2004-01-01
    End date: 2004-12-01

Daclizumab
    Dosage: unspecified
    Indication: Prophylaxis Against Transplant Rejection

Fluconazole
    Dosage: unspecified
    Indication: Mucormycosis

INH
    Indication: Tuberculosis Skin Test Positive
    End date: 2004-12-01

INH
    Dosage: unspecified
    Start date: 2004-12-01

Prednisone
    Dosage: unspecified
    Administration route: Oral
    Indication: Prophylaxis Against Transplant Rejection
    End date: 2004-12-01

Prednisone
    Administration route: Oral
    Start date: 2004-12-01

Rapamune
    Dosage: unspecified
    Administration route: Oral
    Indication: Prophylaxis Against Transplant Rejection
    End date: 2004-12-06

Tacrolimus
    Dosage: unspecified
    Administration route: Oral
    Indication: Prophylaxis Against Transplant Rejection

Voriconazole
    Dosage: unspecified
    Indication: Mucormycosis



Adverse event in female receiving Fluconazole

Reported by a consumer/non-health professional from United States on 2007-10-19

Patient: female, weighing 88.9 kg (195.6 pounds)

Adverse reactions / side effects: Nerve Injury, Movement Disorder, Glossodynia, Hypersensitivity, Respiratory Disorder, Drug Ineffective, Sciatica, Pain, Fall, Chronic Obstructive Pulmonary Disease, Malaise, Upper Respiratory Tract Infection, Fibromyalgia, Pharyngolaryngeal Pain, Toothache, Candidiasis, Muscle Spasms, Dysphagia, Ear Infection, Stress, Joint Injury, Limb Injury, Choking, Lacrimation Increased, Sleep Apnoea Syndrome

Adverse event resulted in: hospitalization, disablity

Suspect drug(s):
Chantix
    Indication: Smoking Cessation Therapy

Fluconazole

Zithromax

Other drugs received by patient: Effexor; Amitriptyline HCL; Buspar; Claritin; Lipitor; Nystatin; Excedrin (Migraine); Provera



Adverse event in 54 year old male receiving Fluconazole

Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-18

Patient: 54 year old male

Adverse reactions / side effects: Spinal Osteoarthritis

Adverse event resulted in: hospitalization

Suspect drug(s):
Fluconazole
    Dosage: 200 mg
    Indication: Pneumonia Cryptococcal
    Start date: 2007-03-29

Mycophenolate Mofetil
    Dosage: 500 mg, bid, oral
    Administration route: Oral
    Indication: Liver Transplant
    Start date: 2006-11-08

Prednisone TAB
    Dosage: 2.5 mg, uid/qd, oral
    Administration route: Oral
    Indication: Liver Transplant
    Start date: 2006-09-13

Prograf
    Dosage: 0.25 mg, bid, oral
    Administration route: Oral
    Indication: Liver Transplant
    Start date: 2006-09-13

Other drugs received by patient: Protonix; Actigall (Urosodeoxycholic Acid); Magnesium Oxide (Magnesium Oxide); Calcium W / Colecalciferol (Colecalciferol, Calcium); Actonel



Adverse event in 50 year old female receiving Fluconazole

Reported by a individual with unspecified qualification from United States on 2007-10-18

Patient: 50 year old female, weighing 100.0 kg (220.0 pounds)

Adverse reactions / side effects: Drug Hypersensitivity

Adverse event resulted in: hospitalization

Suspect drug(s):
Fluconazole

Other drugs received by patient: Nifedipine; Nystatin CR



Adverse event in receiving Fluconazole

Reported by a physician from United States on 2007-10-11

Patient:

Adverse reactions / side effects: Embolism, Hemiplegia, Cardiovascular Disorder, Cerebrovascular Accident, Hypokalaemia

Adverse event resulted in: hospitalization

Suspect drug(s):
Amoxi-Clavulanico
    Dosage: 1 mg, 3 in qd
    Indication: Drug USE FOR Unknown Indication
    Start date: 2007-06-27
    End date: 2007-06-30

Fluconazole
    Dosage: unk
    Indication: Drug USE FOR Unknown Indication
    Start date: 2007-06-27
    End date: 2007-06-28

Metoclopramide
    Dosage: 10 mg in 2 ml, qd
    Indication: Drug USE FOR Unknown Indication
    Start date: 2007-06-27
    End date: 2007-06-30

Pantoprazole Sodium
    Dosage: unk
    Indication: Drug USE FOR Unknown Indication
    Start date: 2007-06-27

Tamsulosine
    Dosage: 0.4 mg, unk
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication
    Start date: 2007-06-28

Verapamil
    Dosage: 3 g, unk
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication
    Start date: 2007-06-27
    End date: 2007-06-29



Adverse event in receiving Fluconazole

Reported by a physician from United States on 2007-10-11

Patient:

Adverse reactions / side effects: Cerebrovascular Accident, Coronary Artery Embolism, Hypokalaemia

Adverse event resulted in: hospitalization

Suspect drug(s):
Amoxi-Clavulanico
    Dosage: 1 mg, 3 in qd
    Indication: Drug USE FOR Unknown Indication
    Start date: 2007-06-27
    End date: 2007-06-30

Fluconazole
    Dosage: unk
    Indication: Drug USE FOR Unknown Indication
    Start date: 2007-06-27
    End date: 2007-06-28

Metoclopramide
    Dosage: 10 mg in 2 ml, qd
    Indication: Drug USE FOR Unknown Indication
    Start date: 2007-06-27
    End date: 2007-06-30

Pantoprazole Sodium
    Dosage: unk
    Indication: Drug USE FOR Unknown Indication
    Start date: 2007-06-27

Tamsulosine
    Dosage: 0.4 mg, unk
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication
    Start date: 2007-06-28

Verapamil
    Dosage: 3 g, unk
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication
    Start date: 2007-06-27
    End date: 2007-06-29



Adverse event in 62 year old male receiving Fluconazole

Reported by a pharmacist from United States on 2007-10-10

Patient: 62 year old male, weighing 113.4 kg (249.5 pounds)

Adverse reactions / side effects: Syncope, Dizziness, Drug Interaction, Orthostatic Hypotension, Asthenia

Adverse event resulted in: hospitalization

Suspect drug(s):
Fluconazole
    Dosage: 400 mg daily po
    Administration route: Oral
    Indication: Meningitis Candida
    Start date: 2007-09-13
    End date: 2007-09-26

Irbesartan
    Dosage: 150 mg daily po
    Administration route: Oral
    Indication: Hypertension
    Start date: 2007-09-15
    End date: 2007-09-26



Adverse event in 43 year old male receiving Fluconazole

Reported by a pharmacist from United States on 2007-10-03

Patient: 43 year old male, weighing 81.2 kg (178.6 pounds)

Adverse reactions / side effects: Hepatic Enzyme Increased

Suspect drug(s):
Fluconazole
    Dosage: 100mg every day po
    Administration route: Oral
    Indication: Oesophageal Candidiasis
    Start date: 2007-01-03
    End date: 2007-04-06

Lopinavir and Ritonavir
    Dosage: 400/100mg bid po
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2007-01-18
    End date: 2007-04-06



Adverse event in 56 year old male receiving Fluconazole

Reported by a individual with unspecified qualification from Italy on 2007-10-03

Patient: 56 year old male

Adverse reactions / side effects: Renal Impairment, Drug Interaction

Adverse event resulted in: hospitalization

Suspect drug(s):
Cyclosporine
    Indication: Immunosuppression

Everolimus (Everolimus)
    Dosage: 3,00 mg (1,5 mg, 2 in 1 d)

Fluconazole
    Indication: Pneumonia

Other drugs received by patient: Ciprofloxacin



Adverse event in 24 year old male receiving Fluconazole

Reported by a individual with unspecified qualification from United States on 2007-07-31

Patient: 24 year old male, weighing 61.2 kg (134.7 pounds)

Adverse reactions / side effects: Refusal of Treatment by Patient, Drug Dose Omission, Vomiting, Diarrhoea, Anaphylactic Reaction, Platelet Count Decreased, Stevens-Johnson Syndrome

Adverse event resulted in: hospitalization

Suspect drug(s):
Bactrim DS
    Dosage: 160mg/800mg daily, oral
    Administration route: Oral
    Indication: Ill-Defined Disorder
    Start date: 2007-06-30
    End date: 2007-07-14

Bactrim DS
    Dosage: 160mg/800mg daily, oral
    Administration route: Oral
    Indication: Pneumocystis Jiroveci Pneumonia
    Start date: 2007-06-30
    End date: 2007-07-14

Fluconazole
    Dosage: once daily, oral
    Administration route: Oral
    Start date: 2007-06-29
    End date: 2007-07-14



Adverse event in female receiving Fluconazole

Reported by a physician from Colombia on 2007-07-26

Patient: female, weighing 50.0 kg (110.0 pounds)

Adverse reactions / side effects: Toxic Epidermal Necrolysis

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Fluconazole
    Dosage: 200 mg daily
    Indication: Systemic Candida
    Start date: 2007-06-15
    End date: 2007-06-23

Tygacil
    Indication: Septic Shock
    Start date: 2007-06-15
    End date: 2007-06-20

Other drugs received by patient: Lovastatin; Glucerna ^abbott^; Cefepime



Adverse event in 55 year old male receiving Fluconazole

Reported by a individual with unspecified qualification from Italy on 2007-07-26

Patient: 55 year old male

Adverse reactions / side effects: Toxic Epidermal Necrolysis, Pyrexia, Acinetobacter Infection, Staphylococcal Infection, Blood Culture Positive, Central Line Infection, Bacterial Infection, Culture Wound Positive

Adverse event resulted in: hospitalization

Suspect drug(s):
Acyclovir
    Indication: non-Hodgkin's Lymphoma

Allopurinol
    Indication: non-Hodgkin's Lymphoma

CO-Trimoxazole (Formulation Unknown) (Generic) (Sulfamethoxazole / Trime
    Indication: non-Hodgkin's Lymphoma

Fluconazole
    Indication: non-Hodgkin's Lymphoma



Adverse event in male receiving Fluconazole

Reported by a individual with unspecified qualification from Australia on 2007-07-25

Patient: male, weighing 78.0 kg (171.6 pounds)

Adverse reactions / side effects: Gastrointestinal Haemorrhage, Hypotension, DRY Skin, Pyrexia, Faeces Discoloured, Renal Impairment, Malaise, Dehydration, Renal Failure Acute

Adverse event resulted in: hospitalization

Suspect drug(s):
Augmentin '125'
    Administration route: Oral
    Indication: Antibiotic Prophylaxis
    Start date: 2005-03-21
    End date: 2005-04-04

Fluconazole
    Administration route: Oral
    Indication: Antibiotic Prophylaxis
    Start date: 2005-03-21
    End date: 2005-04-04

Tipranavir / Ritonavir Capsules, Softgelatin
    Dosage: tpv/rtv 1000/400 mg/mg
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2004-11-19
    End date: 2005-04-27

Warfarin Sodium
    Administration route: Oral
    Indication: Anticoagulant Therapy
    Start date: 2005-02-23

Other drugs received by patient: Lamivudine; Carvedilol; Fludrocortisone Acetate; Pravastatin; Mirtazapine; Centrum; Felodopine; Iron Supplement; Ascorbic Acid; Losec; Thiamine; Cortisone Acetate; Azithromycin; Bactrim; UK 427 / Placebo; Lamivudine; Enfuvirtide; Didanosine; Lopinavir and Ritonavir; Hydrazole Cream; Didanosine; Augmentin DUO Fort; Fluconazole

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