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Prograf (Tacrolimus) - Disability - Suspected Cause - Side Effect Reports

 
 



Index of reports > Disability (67)

Below is the selection of side effect reports (a.k.a. adverse event reports) related to Prograf (Tacrolimus) disability. The selected reports were submitted to the FDA during the sample period of about a year.

 Reports 1 - 30 of 67   Next >>

Possible Prograf side effects in female

Reported by a physician from United States on 2012-08-21

Patient: female, weighing 52.0 kg (114.4 pounds)

Reactions: Fungal Abscess Central Nervous System, Diabetes Mellitus, Mental Status Changes, Fatigue, Hypocalcaemia, Decreased Appetite, Vomiting, Nausea, Hyperglycaemia, Urinary Tract Infection, Convulsion, Lower Respiratory Tract Infection Fungal, Respiratory Failure, Diarrhoea, Dehydration, Hypophagia, Sepsis, Hyperosmolar State, Diabetic Ketoacidosis, Septic Shock, Asthenia

Adverse event resulted in: life threatening event, hospitalization, disablity

Drug(s) suspected as cause:
Certican
    Dosage: 0.75 mg, bid
    Administration route: Oral
    Indication: Renal Transplant
    Start date: 2010-11-21
    End date: 2011-01-11

Prograf
    Dosage: 2 mg, bid
    Administration route: Oral
    Indication: Renal Transplant
    Start date: 2010-11-21

Other drugs received by patient: Prednisone; Prednisone; Insulin; Prednisone



Possible Prograf side effects in female

Reported by a physician from Germany on 2012-08-09

Patient: female, weighing 64.0 kg (140.8 pounds)

Reactions: Liver Function Test Abnormal, Hepatic Cirrhosis

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Prograf
    Dosage: unk
    Administration route: Oral
    Indication: Renal Transplant
    Start date: 2007-02-01
    End date: 2008-08-01

Tacrolimus
    Dosage: unk
    Administration route: Oral
    Indication: Renal Transplant
    Start date: 2008-08-01
    End date: 2012-03-01

Other drugs received by patient: Myfortic; Cellcept



Possible Prograf side effects in male

Reported by a consumer/non-health professional from United States on 2012-08-06

Patient: male, weighing 77.0 kg (169.4 pounds)

Reactions: Depression, Disability

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Prograf



Possible Prograf side effects in female

Reported by a physician from Germany on 2012-07-31

Patient: female, weighing 64.0 kg (140.8 pounds)

Reactions: Liver Function Test Abnormal, Hepatic Cirrhosis

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Prograf
    Dosage: unk
    Administration route: Oral
    Indication: Renal Transplant
    Start date: 2007-02-01
    End date: 2008-08-01

Tacrolimus
    Dosage: unk
    Administration route: Oral
    Indication: Renal Transplant
    Start date: 2008-08-01
    End date: 2012-03-01

Other drugs received by patient: Cellcept; Myfortic



Possible Prograf side effects in male

Reported by a physician from France on 2012-07-27

Patient: male, weighing 90.0 kg (198.0 pounds)

Reactions: Weight Decreased, Hyperkalaemia, Diabetes Mellitus, Off Label Use, Renal Failure, Fatigue, Visual Impairment, Dehydration, Hyperosmolar State, Diabetic Hyperosmolar Coma

Adverse event resulted in: life threatening event, hospitalization, disablity

Drug(s) suspected as cause:
Prograf
    Dosage: 3.5 mg, bid
    Administration route: Oral
    Indication: Nephrotic Syndrome
    Start date: 2011-10-30
    End date: 2011-12-30

Prograf
    Dosage: 3 mg, bid
    Administration route: Oral
    Start date: 2011-12-31
    End date: 2012-01-16

Other drugs received by patient: Irbesartan; Prednisone TAB; Prednisone TAB; Allopurinol; Ezetimibe; Perindopril Erbumine



Possible Prograf side effects in male

Reported by a physician from United States on 2012-07-24

Patient: male

Reactions: Anion GAP Increased, Chapped Lips, Blood Albumin Decreased, Burkitt's Lymphoma Stage II, White Blood Cell Count Increased, Blood Alkaline Phosphatase Decreased, Hypotension, Small Intestinal Obstruction, Blood Phosphorus Decreased, Aspartate Aminotransferase Increased, Epstein-Barr Virus Test Positive, Atelectasis, Blood Magnesium Decreased, Constipation, Electrolyte Depletion, Somnolence, Blood Calcium Decreased, Haematocrit Decreased, RED Blood Cell Count Decreased, Blood Uric Acid Increased, Pleural Effusion, Blood Sodium Decreased, Blood Glucose Increased, Intussusception, Nausea, LIP DRY, Blood Chloride Decreased, Febrile Neutropenia, Protein Total Decreased, Ascites, Immunosuppressant Drug Level Decreased, Renal Failure, Blood Potassium Decreased, Sepsis, Heart Rate Increased, Carbon Dioxide Decreased, Alanine Aminotransferase Decreased, Hypertension

Adverse event resulted in: life threatening event, hospitalization, disablity

Drug(s) suspected as cause:
Elidel
    Dosage: (df topical)
    Administration route: Topical
    Indication: Dermatitis Atopic

Imuran
    Dosage: (50 mg qd)
    Indication: Product Used FOR Unknown Indication

Prograf
    Dosage: (2 mg bid)
    Indication: Product Used FOR Unknown Indication

Singulair
    Dosage: ( 4 mg 4d)
    Indication: Multiple Allergies

Other drugs received by patient: Sodium Chloride; Izofran / 00955301 /; Ventolin HFA; Aloprim; Protonix; Valium; Hydromorphone Hydrochloride; Dilaudid; Nubain; Narcan; D-51 / 2 NS + KCL; Mefoxin



Possible Prograf side effects in male

Reported by a physician from Japan on 2012-06-26

Patient: male, weighing 62.1 kg (136.6 pounds)

Reactions: Interstitial Lung Disease, Drug Ineffective FOR Unapproved Indication, Upper Respiratory Tract Inflammation, Pulmonary Artery Thrombosis

Adverse event resulted in: life threatening event, hospitalization, disablity

Drug(s) suspected as cause:
Betamethasone
    Dosage: unk
    Administration route: Oral
    Start date: 2010-07-09

Betamethasone
    Dosage: 3 mg, unknown/d
    Administration route: Oral
    Indication: Interstitial Lung Disease

Levofloxacin
    Dosage: 500 mg, uid/qd
    Administration route: Oral
    Indication: Upper Respiratory Tract Inflammation
    Start date: 2010-11-05
    End date: 2010-11-11

Prednisolone
    Dosage: 27.5 mg, uid/qd
    Administration route: Oral

Prednisolone
    Dosage: unk
    Administration route: Oral
    Indication: Interstitial Lung Disease

Prednisolone
    Dosage: 30 mg, uid/qd
    Administration route: Oral
    Start date: 2010-04-14
    End date: 2010-07-09

Prograf
    Dosage: 3 mg, uid/qd
    Administration route: Oral
    Indication: Interstitial Lung Disease
    Start date: 2010-05-13

Prograf
    Dosage: 1 mg, uid/qd
    Administration route: Oral
    Start date: 2010-04-30
    End date: 2010-05-06

Prograf
    Dosage: 2 mg, uid/qd
    Administration route: Oral
    Start date: 2010-05-07
    End date: 2010-05-12

Other drugs received by patient: Flaveric; Maglax; Warfarin Sodium; Codeine Phosphate; Urokinase; Nizatidine; Lasix; Heparin Calcium; Heparin Calcium; Cotrim; Mucosolvan; Gastrom; Mucodyne; Urokinase; Warfarin Sodium



Possible Prograf side effects in male

Reported by a physician from Japan on 2012-06-21

Patient: male, weighing 62.1 kg (136.6 pounds)

Reactions: Interstitial Lung Disease, Drug Ineffective FOR Unapproved Indication, Upper Respiratory Tract Inflammation, Pulmonary Artery Thrombosis

Adverse event resulted in: life threatening event, hospitalization, disablity

Drug(s) suspected as cause:
Betamethasone
    Dosage: unk
    Administration route: Oral
    Start date: 2010-07-09

Betamethasone
    Dosage: 3 mg, unknown/d
    Administration route: Oral
    Indication: Interstitial Lung Disease

Prednisolone
    Dosage: unk mg, uid/qd
    Administration route: Oral
    End date: 2010-07-09

Prednisolone
    Dosage: 30 mg, unknown/d
    Administration route: Oral

Prednisolone
    Dosage: 30 mg, uid/qd
    Administration route: Oral
    Indication: Interstitial Lung Disease
    Start date: 2010-04-14

Prednisolone
    Dosage: 27.5 mg, unknown/d
    Administration route: Oral

Prograf
    Dosage: 3 mg, uid/qd
    Administration route: Oral
    Start date: 2010-05-13

Prograf
    Dosage: 1 mg, uid/qd
    Administration route: Oral
    Indication: Interstitial Lung Disease
    Start date: 2010-04-30
    End date: 2010-05-06

Prograf
    Dosage: 2 mg, uid/qd
    Administration route: Oral
    Start date: 2010-05-07
    End date: 2010-05-12

Other drugs received by patient: Nizatidine; Urokinase; Codeine Phosphate; Heparin Calcium; Flaveric; Lasix; Mucodyne; Urokinase; Warfarin Sodium; Gastrom; Levofloxacin; Heparin Calcium; Cotrim; Mucosolvan; Maglax; Warfarin Sodium



Possible Prograf side effects in 38 year old female

Reported by a individual with unspecified qualification from United States on 2012-06-15

Patient: 38 year old female, weighing 61.2 kg (134.7 pounds)

Reactions: Renal Failure, Nephropathy Toxic, Hypertension

Adverse event resulted in: life threatening event, disablity

Drug(s) suspected as cause:
Prograf
    Dosage: 2 mg once day
    Indication: Prophylaxis Against Transplant Rejection
    Start date: 2005-12-01
    End date: 2011-06-01

Prograf
    Dosage: 2 mg once day
    Indication: Transplant
    Start date: 2005-12-01
    End date: 2011-06-01



Possible Prograf side effects in male

Reported by a consumer/non-health professional from France on 2012-06-12

Patient: male

Reactions: Adverse Drug Reaction

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Prograf
    Dosage: 2 mg, unknown/d
    Administration route: Oral
    Indication: Renal Transplant

Prograf
    Dosage: 3 mg, unknown/d
    Start date: 2010-07-19

Prograf
    Dosage: 3 mg, unknown/d
    Start date: 2011-07-13

Prograf
    Dosage: 3 mg, unknown/d
    Start date: 2011-04-15

Prograf
    Dosage: 2 mg, unknown/d
    Start date: 2011-09-12

Prograf
    Dosage: 3 mg, unknown/d
    Start date: 2011-07-04

Other drugs received by patient: Corticosteroid NOS



Possible Prograf side effects in female

Reported by a physician from Germany on 2012-05-24

Patient: female, weighing 42.0 kg (92.4 pounds)

Reactions: Optic Atrophy

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Imatinib Mesylate
    Dosage: 600 mg, unk
    Administration route: Oral
    Indication: Acute Lymphocytic Leukaemia
    Start date: 2012-01-02
    End date: 2012-03-13

Prograf
    Indication: Acute Lymphocytic Leukaemia

Other drugs received by patient: Cotrim DS; Acyclovir; Lyrica



Possible Prograf side effects in male

Reported by a physician from France on 2012-05-18

Patient: male, weighing 90.0 kg (198.0 pounds)

Reactions: Weight Decreased, Hyperkalaemia, Diabetes Mellitus, Off Label Use, Renal Failure, Fatigue, Visual Impairment, Dehydration, Hyperosmolar State, Diabetic Hyperosmolar Coma

Adverse event resulted in: life threatening event, hospitalization, disablity

Drug(s) suspected as cause:
Prograf
    Dosage: 3 mg, bid
    Administration route: Oral
    Start date: 2011-12-31
    End date: 2012-01-16

Prograf
    Dosage: 3.5 mg, bid
    Administration route: Oral
    Indication: Nephrotic Syndrome
    Start date: 2011-10-30
    End date: 2011-12-30

Other drugs received by patient: Prednisone TAB; Prednisone TAB; Perindopril Erbumine; Ezetimibe; Irbesartan; Allopurinol



Possible Prograf side effects in female

Reported by a consumer/non-health professional from France on 2012-05-17

Patient: female

Reactions: Adverse Drug Reaction, Adverse Event

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Prograf
    Dosage: 2 mg, unknown/d
    Indication: Renal Transplant

Tacrolimus
    Dosage: unk
    Indication: Renal Transplant



Possible Prograf side effects in female

Reported by a pharmacist from United States on 2012-05-16

Patient: female

Reactions: Pneumonia, Mental Status Changes, Pyrexia, Cerebrovascular Accident, Convulsion

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Prograf



Possible Prograf side effects in 40 year old female

Reported by a physician from Japan on 2012-05-15

Patient: 40 year old female

Reactions: Cerebral Infarction, Posterior Reversible Encephalopathy Syndrome, Drug Prescribing Error

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Prograf



Possible Prograf side effects in female

Reported by a consumer/non-health professional from France on 2012-05-15

Patient: female

Reactions: Medication Error, Adverse Drug Reaction

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Prograf
    Dosage: 8 mg, unknown/d
    Indication: Liver Transplant

Tacrolimus
    Dosage: 8 mg, unknown/d
    Indication: Liver Transplant
    Start date: 2011-10-28

Tacrolimus
    Dosage: 7 mg, unknown/d

Other drugs received by patient: Corticosteroid NOS



Possible Prograf side effects in 75 year old female

Reported by a health professional (non-physician/pharmacist) from Switzerland on 2012-04-18

Patient: 75 year old female

Reactions: Staphylococcal Infection, Drug Interaction, Renal Failure Chronic

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Prograf

Other drugs received by patient possibly interacting with the suspect drug:
Floxapen
    Dosage: 2 g, tid
    Indication: Staphylococcal Infection
    Start date: 2011-03-19
    End date: 2011-03-30

Prograf
    Dosage: 3 mg, uid/qd
    Administration route: Oral
    Start date: 2010-12-09

Prograf
    Dosage: 3.5 mg, uid/qd
    Administration route: Oral
    Start date: 2011-03-25

Prograf
    Dosage: 4 mg, uid/qd
    Administration route: Oral
    Start date: 2011-12-08

Prograf
    Dosage: 3 mg, uid/qd
    Administration route: Oral
    Start date: 2012-01-03

Prograf
    Dosage: 6 mg, uid/qd
    Administration route: Oral
    Start date: 2011-04-01

Prograf
    Dosage: 4 mg, uid/qd
    Administration route: Oral
    Start date: 2011-04-08

Prograf
    Dosage: 3 mg, uid/qd
    Administration route: Oral
    Start date: 2011-03-21

Prograf
    Dosage: 4 mg, uid/qd
    Administration route: Oral
    Start date: 2011-06-03

Other drugs received by patient: Allopurinol; Tenormin; Amiloride HCL and Hydrochlorothiazide; Marcumar; Zestril



Possible Prograf side effects in 75 year old female

Reported by a health professional (non-physician/pharmacist) from Switzerland on 2012-04-12

Patient: 75 year old female

Reactions: Drug Interaction, Renal Failure Chronic

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Prograf

Other drugs received by patient possibly interacting with the suspect drug:
Floxapen
    Dosage: 2 g, tid
    Indication: Staphylococcal Infection
    Start date: 2011-03-19
    End date: 2011-03-30

Prograf
    Dosage: 6 mg, uid/qd
    Administration route: Oral
    Start date: 2011-04-02
    End date: 2011-04-08

Prograf
    Dosage: 3 mg, uid/qd
    Administration route: Oral
    Start date: 2011-12-08

Prograf
    Dosage: 3.5 mg, uid/qd
    Administration route: Oral
    Start date: 2011-03-26
    End date: 2011-04-01

Prograf
    Dosage: 3.5 mg, uid/qd
    Administration route: Oral
    Start date: 2011-03-25

Prograf
    Dosage: 4 mg, uid/qd
    Administration route: Oral
    Start date: 2011-04-07
    End date: 2011-12-08

Other drugs received by patient: Amiloride HCL and Hydrochlorothiazide; Marcumar; Allopurinol; Zestril; Tenormin



Possible Prograf side effects in male

Reported by a consumer/non-health professional from United States on 2012-04-11

Patient: male, weighing 72.6 kg (159.7 pounds)

Reactions: Cerebral Disorder, Poisoning

Adverse event resulted in: life threatening event, hospitalization, disablity

Drug(s) suspected as cause:
Prograf



Possible Prograf side effects in male

Reported by a consumer/non-health professional from United States on 2012-04-09

Patient: male, weighing 85.0 kg (187.0 pounds)

Reactions: Renal Disorder, Iatrogenic Injury, Abasia, Anxiety, Neuropathy Peripheral, Intestinal Perforation, Dysgraphia, Memory Impairment, Intracranial Aneurysm, Disability

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Flagyl
    Dosage: unk
    Indication: Product Used FOR Unknown Indication

Prograf
    Dosage: 2 mg, bid
    Administration route: Oral
    Indication: Liver Transplant
    Start date: 2001-01-01



Possible Prograf side effects in female

Reported by a physician from Germany on 2012-04-03

Patient: female, weighing 42.0 kg (92.4 pounds)

Reactions: Optic Atrophy

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Imatinib Mesylate
    Dosage: 600 mg, unk
    Indication: Acute Lymphocytic Leukaemia
    Start date: 2012-01-02
    End date: 2012-03-13

Prograf
    Indication: Acute Lymphocytic Leukaemia

Other drugs received by patient: Panthenol; Cotrim DS; Acyclovir; Lyrica



Possible Prograf side effects in male

Reported by a physician from Japan on 2012-03-27

Patient: male, weighing 54.0 kg (118.8 pounds)

Reactions: Multi-Organ Failure, Renal Failure, Respiratory Failure, Septic Shock

Adverse event resulted in: life threatening event, disablity

Drug(s) suspected as cause:
Prograf

Other drugs received by patient: Glakay; Asacol; Famotidine; Miya BM; Prednisolone; Ferrous Citrate; Loperamide HCL



Possible Prograf side effects in female

Reported by a physician from Germany on 2012-03-23

Patient: female, weighing 42.0 kg (92.4 pounds)

Reactions: Optic Atrophy

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Imatinib Mesylate
    Dosage: 600 mg, unk
    Indication: Acute Lymphocytic Leukaemia
    Start date: 2012-01-02
    End date: 2012-03-13

Prograf
    Indication: Acute Lymphocytic Leukaemia

Other drugs received by patient: Panthenol; Acyclovir; Cotrim DS; Lyrica



Possible Prograf side effects in male

Reported by a consumer/non-health professional from United States on 2012-03-22

Patient: male, weighing 85.0 kg (187.0 pounds)

Reactions: Anxiety, Hospitalisation, Abasia, Memory Impairment, Disability, Brain Operation

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Prograf



Possible Prograf side effects in male

Reported by a physician from Japan on 2012-03-20

Patient: male

Reactions: Drug Interaction, Loss of Consciousness

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Prograf

Other drugs received by patient possibly interacting with the suspect drug:
Depas
    Dosage: 2 df, prn
    Administration route: Oral

Other drugs received by patient: Mycophenolate Mofetil (Cellcept); Steroid



Possible Prograf side effects in female

Reported by a physician from United States on 2012-03-16

Patient: female

Reactions: Death, Pneumonia

Adverse event resulted in: death, disablity

Drug(s) suspected as cause:
Prograf
    Dosage: 4 mg, uid/qd
    Administration route: Oral
    Indication: Renal Transplant
    Start date: 2005-11-15

Prograf
    Dosage: 2 mg, bid
    Administration route: Oral
    Start date: 2005-11-15

Other drugs received by patient: Mycophenolate Mofetil (Cellcept)



Possible Prograf side effects in male

Reported by a physician from Japan on 2012-03-13

Patient: male, weighing 8.1 kg (17.8 pounds)

Reactions: Food Allergy, Gastroenteritis Eosinophilic

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Prograf

Other drugs received by patient: Fludarabine Phosphate; Prednisolone; Cyclosporine; Methotrexate; Decadron; Anti-Thymocyte Globulin NOS; Melphalan Hydrochloride; Prednisolone; Prednisolone



Possible Prograf side effects in 64 year old female

Reported by a physician from United States on 2012-03-09

Patient: 64 year old female, weighing 56.7 kg (124.7 pounds)

Reactions: Impaired Driving Ability, Dysgraphia, Tremor

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Cellcept
    Dosage: 500 mg, tid, oral
    Administration route: Oral
    Indication: Transplant
    Start date: 2007-01-01

Prednisone
    Dosage: 5 mg, qd, oral
    Administration route: Oral
    Indication: Transplant
    Start date: 2007-01-01

Prograf
    Dosage: 1 mg, qd, oral
    Administration route: Oral
    Indication: Transplant
    Start date: 2007-01-01

Ursodiol
    Dosage: 500 mg, bid,oral
    Administration route: Oral
    Indication: Biliary Cirrhosis Primary
    Start date: 2007-01-01

Other drugs received by patient: Amlodipine



Possible Prograf side effects in female

Reported by a health professional (non-physician/pharmacist) from United States on 2012-03-08

Patient: female, weighing 52.0 kg (114.4 pounds)

Reactions: Fungal Abscess Central Nervous System, Diabetes Mellitus, Mental Status Changes, Fatigue, Hypocalcaemia, Decreased Appetite, Vomiting, Nausea, Urinary Tract Infection, Hyperglycaemia, Convulsion, Respiratory Failure, Lower Respiratory Tract Infection Fungal, Diarrhoea, Dehydration, Sepsis, Hypophagia, Hyperosmolar State, Diabetic Ketoacidosis, Asthenia, Septic Shock

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Certican
    Dosage: 0.75 mg, bid
    Administration route: Oral
    Indication: Renal Transplant
    Start date: 2010-11-21
    End date: 2011-01-11

Prograf
    Dosage: 2 mg, bid
    Administration route: Oral
    Indication: Renal Transplant
    Start date: 2010-11-21

Other drugs received by patient: Prednisone TAB; Prednisone TAB; Insulin; Prednisone TAB



Possible Prograf side effects in 9 year old female

Reported by a physician from Japan on 2012-03-07

Patient: 9 year old female

Reactions: Ventricular Extrasystoles, Blood Bilirubin Increased, Weight Increased, Haemoglobin Decreased, Renal Failure, Respiratory Failure, Dialysis, Blood Potassium Decreased, Pulmonary Congestion, Pleural Effusion, Platelet Count Decreased, Neuroblastoma Recurrent, Pulmonary Oedema, Cardiac Arrest

Adverse event resulted in: death, life threatening event, disablity

Drug(s) suspected as cause:
Ambisome
    Dosage: 49.2 mg, uid/qd, parenteral; 50 mg, uid/qd, parenteral
    Indication: Pyelonephritis Fungal
    Start date: 2008-04-23
    End date: 2008-04-25

Ambisome
    Dosage: 49.2 mg, uid/qd, parenteral; 50 mg, uid/qd, parenteral
    Indication: Pyelonephritis Fungal
    Start date: 2008-04-09
    End date: 2008-04-22

Anitvirals FOR Systemic USE (Antivirals FOR Systemic Use)
    Dosage: iv nos; iv nos; iv nos
    Indication: Viral Infection
    Start date: 2008-05-06
    End date: 2008-05-06

Anitvirals FOR Systemic USE (Antivirals FOR Systemic Use)
    Dosage: iv nos; iv nos; iv nos
    Indication: Viral Infection
    Start date: 2008-04-23
    End date: 2008-04-23

Anitvirals FOR Systemic USE (Antivirals FOR Systemic Use)
    Dosage: iv nos; iv nos; iv nos
    Indication: Viral Infection
    Start date: 2008-05-10
    End date: 2008-05-10

Foscavir
    Dosage: parenteral
    Indication: Cytomegalovirus Infection
    Start date: 2008-04-15
    End date: 2008-04-22

Neutrogin (Lenograstim)
    Dosage: 100 ug, uid/qd, iv nos; dr, parenteral
    Indication: Neutropenia
    Start date: 2008-04-15
    End date: 2008-04-26

Neutrogin (Lenograstim)
    Dosage: 100 ug, uid/qd, iv nos; dr, parenteral
    Indication: Neutropenia
    Start date: 2008-04-27
    End date: 2008-04-30

Prograf
    Dosage: 0.1 mg, unknown/d, parenteral
    Indication: Graft Versus Host Disease
    End date: 2008-04-27

Targpocid (Teicoplanin)
    Dosage: parenteral
    Indication: Infection
    Start date: 2008-04-20
    End date: 2008-04-25

Other drugs received by patient: Vfend; Solu-Medrol; Nicardipine Hydrochloride; Sodium Chloride 0.9%; Atraxa-P (Hydroxyzine Hydrochloride); Capillary Stablizing Agents; Amoban (Zopiclone); Elemenmic (Minerals Nos); Potassium Chloride; Omepral (Omperazole); Morphine Hydrochloride (Morphine Hydrochloride); Urso (Ursodexoycholic Acid); Dopamine Hydrochloride; Firstcin (Cefozopran Hydrochloride); Fulcaliq 2; Novo Heparin Calcium (Heparin Calcium); Sulfamethoxazole and Trimethoprim; Alprostadil; Albumin (Human)



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