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Prednisolone (Prednisolone) - Herpes Zoster - Suspected Cause - Side Effect Reports

 
 



Index of reports > Cases with Herpes Zoster (89)

Below is the selection of side effect reports (a.k.a. adverse event reports) related to Prednisolone where reactions include herpes zoster. The selected reports were submitted to the FDA during the sample period of about a year.

 Reports 1 - 30 of 89   Next >>

Possible Prednisolone side effects in female

Reported by a physician from Japan on 2012-08-27

Patient: female, weighing 51.0 kg (112.2 pounds)

Reactions: Pneumonia, Cholecystitis Acute, Pyrexia, Enterocolitis, Herpes Zoster

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Inc424
    Dosage: 30 mg, bid
    Administration route: Oral
    Indication: Myelofibrosis
    Start date: 2011-12-12
    End date: 2012-03-31

Inc424
    Dosage: unk
    Administration route: Oral
    Start date: 2012-04-02
    End date: 2012-04-09

Inc424
    Dosage: 20 mg, qd
    Start date: 2012-05-25
    End date: 2012-08-18

Prednisolone
    Dosage: 10 mg, qd
    Administration route: Oral
    Indication: Platelet Count Decreased
    Start date: 2004-05-18

Other drugs received by patient: Lasix; MS Contin; Acetaminophen; Merislon; Lansoprazole; Exjade; Pursennid; Terranas; Amoban; Acetaminophen; Maxalt; Alosenn; Laxoberon; Celecoxib; Lyrica; Exjade; Morphine; Halcion; Magnesium Oxide; Vitamin B12; Uloric



Possible Prednisolone side effects in 32 year old male

Reported by a physician from Japan on 2012-08-17

Patient: 32 year old male, weighing 57.0 kg (125.4 pounds)

Reactions: Upper Respiratory Tract Inflammation, Herpes Zoster, Renal Impairment, Oral Candidiasis, Neoplasm Skin, Bronchitis, White Blood Cell Count Increased, Influenza

Drug(s) suspected as cause:
Micardis
    Dosage: 40 mg
    Administration route: Oral
    Start date: 2007-06-24
    End date: 2007-08-01

Micardis
    Dosage: 80 mg
    Administration route: Oral
    Start date: 2007-08-02

Micardis
    Dosage: 20 mg
    Administration route: Oral
    Indication: Hypertension
    Start date: 2007-06-08
    End date: 2007-06-23

Prednisolone
    Dosage: 50 mg
    Administration route: Oral
    Indication: Lupus Nephritis
    Start date: 2007-05-31

Prograf
    Dosage: 1.5 mg
    Administration route: Oral
    Indication: Lupus Nephritis
    Start date: 2007-05-31
    End date: 2007-06-11

Prograf
    Dosage: 2 mg
    Administration route: Oral
    Start date: 2007-06-12

Other drugs received by patient: Pravastatin; Zantac; Alfarol; Bonalon 5MG; Warfarin Sodium; Vitamin B12



Possible Prednisolone side effects in female

Reported by a health professional (non-physician/pharmacist) from Japan on 2012-08-16

Patient: female, weighing 51.0 kg (112.2 pounds)

Reactions: Pneumonia, Cholecystitis Acute, Pyrexia, Herpes Zoster

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Inc424
    Dosage: unk
    Administration route: Oral
    Start date: 2012-04-02
    End date: 2012-04-09

Inc424
    Dosage: 20 mg, qd
    Start date: 2012-05-25

Inc424
    Dosage: 30 mg, bid
    Administration route: Oral
    Indication: Myelofibrosis
    Start date: 2011-12-12
    End date: 2012-03-31

Prednisolone
    Dosage: 10 mg, qd
    Administration route: Oral
    Indication: Platelet Count Decreased
    Start date: 2004-05-18

Other drugs received by patient: Exjade; Vitamin B12; Halcion; Lansoprazole; Lasix; Celecoxib; Alosenn; Terranas; MS Contin; Maxalt; Amoban; Exjade; Acetaminophen; Uloric; Merislon; Magnesium Oxide; Pursennid; Laxoberon; Morphine; Acetaminophen; Lyrica



Possible Prednisolone side effects in 77 year old female

Reported by a physician from Japan on 2012-08-01

Patient: 77 year old female, weighing 36.0 kg (79.2 pounds)

Reactions: Blood Alkaline Phosphatase Increased, Back Pain, Blood Urea Increased, Pneumonia, Pubis Fracture, Urinary Tract Infection, General Physical Health Deterioration, Herpes Zoster, Renal Impairment, Sepsis, Dehydration, Neutropenia, Thrombocytopenia, Blood Creatinine Increased

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Exjade
    Dosage: 625 mg, qd
    Administration route: Oral
    Start date: 2011-05-07
    End date: 2011-05-18

Exjade
    Dosage: 625 mg, on alternate days
    Administration route: Oral
    Start date: 2011-05-19

Exjade
    Dosage: 750 mg, qd
    Administration route: Oral
    Indication: Myelodysplastic Syndrome
    Start date: 2009-09-16
    End date: 2011-04-03

Prednisolone
    Dosage: 5 mg daily
    Administration route: Oral
    Start date: 2010-04-22

Prednisolone
    Dosage: 8 mg, daily
    Administration route: Oral
    End date: 2009-09-29

Prednisolone
    Dosage: 7 mg, daily
    Administration route: Oral
    Start date: 2009-09-30
    End date: 2010-02-02

Prednisolone
    Dosage: 6 mg, daily
    Administration route: Oral
    Start date: 2010-02-03
    End date: 2010-04-21

Prednisolone
    Dosage: 4 mg, unk
    Administration route: Oral

Revlimid
    Dosage: 5 mg, daily
    Administration route: Oral
    Indication: Myelodysplastic Syndrome
    Start date: 2011-04-12
    End date: 2011-05-02

Revlimid
    Dosage: 5 mg, daily
    Administration route: Oral
    Start date: 2011-05-19
    End date: 2011-06-01

Other drugs received by patient: Equa; Xalatan; Desferal; Famotidine; Novolin R; RED Blood Cells, Concentrated; Glufast; Novolin R; RED Blood Cells, Concentrated; Alendronate Sodium; Timoptol-XE; Platelets; Novolin R; Amaryl; Novolin R; Azopt; Platelets; Famotidine; Glufast; Clarithromycin; Desferal; Desferal; Mucodyne; Voglibose



Possible Prednisolone side effects in 77 year old female

Reported by a physician from Japan on 2012-08-01

Patient: 77 year old female, weighing 36.0 kg (79.2 pounds)

Reactions: Blood Alkaline Phosphatase Increased, Back Pain, Pneumonia, Blood Urea Increased, Pubis Fracture, Urinary Tract Infection, General Physical Health Deterioration, Herpes Zoster, Renal Impairment, Sepsis, Dehydration, Neutropenia, Thrombocytopenia, Blood Creatinine Increased

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Exjade
    Dosage: 750 mg, qd
    Administration route: Oral
    Indication: Myelodysplastic Syndrome
    Start date: 2009-09-16
    End date: 2011-04-03

Exjade
    Dosage: 625 mg, on alternate days
    Administration route: Oral
    Start date: 2011-05-19

Exjade
    Dosage: 625 mg, qd
    Administration route: Oral
    Start date: 2011-05-07
    End date: 2011-05-18

Prednisolone
    Dosage: 8 mg, daily
    Administration route: Oral
    End date: 2009-09-29

Prednisolone
    Dosage: 7 mg, daily
    Administration route: Oral
    Start date: 2009-09-30
    End date: 2010-02-02

Prednisolone
    Dosage: 6 mg, daily
    Administration route: Oral
    Start date: 2010-02-03
    End date: 2010-04-21

Prednisolone
    Dosage: 4 mg, unk
    Administration route: Oral

Prednisolone
    Dosage: 5 mg daily
    Administration route: Oral
    Start date: 2010-04-22

Revlimid
    Dosage: 5 mg, daily
    Administration route: Oral
    Indication: Myelodysplastic Syndrome
    Start date: 2011-04-12
    End date: 2011-05-02

Revlimid
    Dosage: 5 mg, daily
    Administration route: Oral
    Start date: 2011-05-19
    End date: 2011-06-01

Other drugs received by patient: Platelets; Novolin R; Clarithromycin; Xalatan; Desferal; Novolin R; RED Blood Cells, Concentrated; Mucodyne; Famotidine; Famotidine; Azopt; Platelets; Desferal; RED Blood Cells, Concentrated; Alendronate Sodium; Voglibose; Timoptol-XE; Amaryl; Novolin R; Novolin R; Glufast; Glufast; Desferal; Equa



Possible Prednisolone side effects in male

Reported by a physician from Japan on 2012-07-18

Patient: male

Reactions: Bronchopneumonia, Disseminated Intravascular Coagulation, Pyrexia, Constipation, Herpes Zoster, Neuropathy Peripheral, C-Reactive Protein Increased, Thrombocytopenia, Blood Creatinine Increased, Cardiac Failure Congestive, Decreased Appetite, Prothrombin Time Ratio Increased, Dyspnoea, Pneumonia, Anaemia, Muscular Weakness, Lobar Pneumonia, Haemoglobin Decreased, Cerebral Infarction, Sepsis, Platelet Count Decreased, Neutropenia, Neutrophil Count Decreased

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

Drug(s) suspected as cause:
Dexamethasone
    Dosage: 2.8571 milligram
    Administration route: Oral
    Start date: 2012-01-13
    End date: 2012-02-03

Dexamethasone
    Dosage: 2.8571 milligram
    Administration route: Oral
    Indication: Multiple Myeloma
    Start date: 2011-12-10
    End date: 2012-01-07

Prednisolone
    Dosage: 5 milligram
    Administration route: Oral
    Start date: 2011-05-12
    End date: 2011-05-25

Prednisolone
    Dosage: 60 milligram
    Administration route: Oral
    Start date: 2011-05-26
    End date: 2011-06-01

Prednisolone
    Dosage: 10 milligram
    Indication: Multiple Myeloma
    Start date: 2012-02-09
    End date: 2012-02-17

Prednisolone
    Dosage: 5 milligram
    Administration route: Oral
    Start date: 2011-03-31
    End date: 2011-04-13

Prednisolone
    Dosage: 60 milligram
    Administration route: Oral
    Indication: Multiple Myeloma
    Start date: 2011-03-24
    End date: 2011-03-30

Prednisolone
    Dosage: 10 milligram
    Administration route: Oral
    Start date: 2011-08-17
    End date: 2012-02-08

Prednisolone
    Dosage: 60 milligram
    Administration route: Oral
    Start date: 2011-04-21
    End date: 2011-05-11

Revlimid
    Dosage: 15 milligram
    Administration route: Oral
    Indication: Multiple Myeloma
    Start date: 2011-03-24
    End date: 2011-04-13

Revlimid
    Dosage: 5 milligram
    Administration route: Oral
    Start date: 2011-08-17
    End date: 2011-09-06

Revlimid
    Dosage: 5 milligram
    Administration route: Oral
    Start date: 2011-09-14
    End date: 2011-10-03

Revlimid
    Dosage: 5 milligram
    Administration route: Oral
    Start date: 2011-10-12
    End date: 2011-10-22

Revlimid
    Dosage: 5 milligram
    Administration route: Oral
    Start date: 2011-12-11
    End date: 2011-12-31

Revlimid
    Dosage: 15 milligram
    Administration route: Oral
    Start date: 2011-04-21
    End date: 2011-05-11

Revlimid
    Dosage: 5 milligram
    Administration route: Oral
    Start date: 2012-01-25
    End date: 2012-02-11

Other drugs received by patient: Glufast; Warfarin Sodium; Famotidine; Mucosta; Flomax; Warfarin Sodium; Magnesium Oxide; Zometa; Lansoprazole; Magnesium Oxide; Slow-K; Glufast; Tamsulosin HCL; Humulin R; Warfarin Sodium; Tamsulosin HCL; SHA-Kanzo-TO; SHA-Kanzo-TO; Levothyroxine Sodium; Diovan; Slow-K; Warfarin Sodium; Mucosta; Diovan; Clarithromycin; Levothyroxine Sodium; Levothyroxine Sodium; Zometa



Possible Prednisolone side effects in female

Reported by a health professional (non-physician/pharmacist) from Japan on 2012-07-17

Patient: female, weighing 51.0 kg (112.2 pounds)

Reactions: Pneumonia, Cholecystitis Acute, Pyrexia, Herpes Zoster

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Inc424
    Dosage: unk
    Administration route: Oral
    Start date: 2012-04-02
    End date: 2012-04-09

Inc424
    Dosage: 20 mg, qd
    Start date: 2012-05-25

Inc424
    Dosage: 30 mg, bid
    Administration route: Oral
    Indication: Myelofibrosis
    Start date: 2011-12-12
    End date: 2012-03-31

Prednisolone
    Dosage: 10 mg, qd
    Administration route: Oral
    Indication: Platelet Count Decreased
    Start date: 2004-05-18

Other drugs received by patient: Halcion; Lyrica; Pursennid; Amoban; Lasix; Morphine; Magnesium Oxide; Exjade; Lansoprazole; Acetaminophen; Vitamin B12; Celecoxib; MS Contin; Acetaminophen



Possible Prednisolone side effects in male

Reported by a physician from Japan on 2012-07-16

Patient: male, weighing 67.0 kg (147.4 pounds)

Reactions: Pneumonia Aspiration, Diabetes Mellitus, Malnutrition, Aspergillosis Oral, Stupor, Herpes Zoster, Ileus, Platelet Count Decreased, Altered State of Consciousness

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Akineton
    Dosage: 3 mg, unk
    Administration route: Oral
    Start date: 2009-08-31
    End date: 2009-09-01

Akineton
    Dosage: 3 mg, unk
    Administration route: Oral
    Start date: 2008-08-14
    End date: 2009-08-24

Certican
    Dosage: 0.5 mg, unk
    Administration route: Oral
    Start date: 2009-08-08
    End date: 2009-08-09

Certican
    Dosage: 0.5 mg, unk
    Administration route: Oral
    Start date: 2009-10-16
    End date: 2009-10-16

Certican
    Dosage: 0.75 mg, unk
    Administration route: Oral
    Start date: 2010-03-09
    End date: 2010-03-15

Certican
    Dosage: 0.5 mg, unk
    Administration route: Oral
    Start date: 2009-10-14
    End date: 2009-10-14

Certican
    Dosage: 0.5 mg, unk
    Administration route: Oral
    Start date: 2010-03-16
    End date: 2010-04-15

Certican
    Dosage: 1.5 mg, unk
    Indication: Heart Transplant
    Start date: 2009-07-30
    End date: 2009-09-01

Certican
    Dosage: 0.75 mg, unk
    Administration route: Oral
    Start date: 2009-08-10

Certican
    Dosage: 1 mg, unk
    Administration route: Oral
    Start date: 2009-08-12
    End date: 2009-08-24

Certican
    Dosage: 1 mg, unk
    Administration route: Oral
    Start date: 2009-10-15
    End date: 2009-10-15

Certican
    Dosage: 1 mg, unk
    Administration route: Oral
    Start date: 2010-02-20
    End date: 2010-03-08

Certican
    Dosage: 1.25 mg, unk
    Administration route: Oral
    Start date: 2009-08-25
    End date: 2009-08-26

Certican
    Dosage: 1 mg, unk
    Administration route: Oral
    Start date: 2009-08-27
    End date: 2009-09-01

Certican
    Dosage: 0.75 mg, unk
    Administration route: Oral
    Start date: 2010-04-16

Certican
    Dosage: 1 mg, unk
    Administration route: Oral
    Start date: 2009-08-07
    End date: 2009-08-07

Clonazepam

Meropenem
    Dosage: unk ukn, unk

Meropenem
    Dosage: 1.5 mg, unk
    Start date: 2009-08-31
    End date: 2009-09-09

Meropenem
    Dosage: 1.5 mg, unk
    Start date: 2009-08-11
    End date: 2009-08-24

Prednisolone
    Dosage: 10 mg, unk
    Administration route: Oral
    Start date: 2009-09-03
    End date: 2010-03-26

Prednisolone
    Dosage: 7.5 mg, unk
    Administration route: Oral
    Start date: 2010-03-27
    End date: 2010-04-01

Prednisolone
    Dosage: 5 mg, unk
    Administration route: Oral
    Start date: 2010-04-24
    End date: 2010-05-01

Prednisolone
    Dosage: unk ukn, unk
    Administration route: Oral
    Start date: 2010-05-28

Prednisolone
    Dosage: 2.5 mg, unk
    Administration route: Oral
    Indication: Heart Transplant
    Start date: 2009-01-06
    End date: 2009-09-02

Prograf
    Dosage: 6 mg, unk
    Administration route: Oral
    Start date: 2009-09-22
    End date: 2009-09-24

Prograf
    Dosage: 6.2 mg, unk
    Administration route: Oral
    Start date: 2009-10-02
    End date: 2009-10-04

Prograf
    Dosage: 4 mg, unk
    Administration route: Oral
    Start date: 2009-08-15
    End date: 2009-08-16

Prograf
    Dosage: 5.4 mg, unk
    Administration route: Oral
    Start date: 2009-09-17
    End date: 2009-09-20

Prograf
    Dosage: 7 mg, daily
    Administration route: Oral
    Start date: 2009-12-16

Prograf
    Dosage: 4.7 mg, unk
    Administration route: Oral
    Start date: 2010-01-28
    End date: 2010-02-15

Prograf
    Dosage: 5.6 mg, unk
    Administration route: Oral
    Start date: 2010-02-16
    End date: 2010-03-25

Prograf
    Dosage: 5.8 mg, unk
    Administration route: Oral
    Start date: 2010-03-26
    End date: 2010-03-27

Prograf
    Dosage: 6 mg, unk
    Administration route: Oral
    Start date: 2010-05-26
    End date: 2010-06-20

Prograf
    Dosage: 6.4 mg, daily

Prograf
    Dosage: 3.7 mg, unk
    Administration route: Oral
    Start date: 2009-08-17
    End date: 2009-09-01

Prograf
    Dosage: 6.5 mg, unk
    Administration route: Oral
    Start date: 2009-09-25
    End date: 2009-10-01

Prograf
    Dosage: 6.4 mg, unk
    Administration route: Oral
    Start date: 2010-01-22
    End date: 2010-01-27

Prograf
    Dosage: 6 mg, unk
    Administration route: Oral
    Start date: 2010-03-28
    End date: 2010-04-06

Prograf
    Dosage: 4.2 mg, unk
    Administration route: Oral
    Start date: 2009-08-10
    End date: 2009-08-14

Prograf
    Dosage: 5 mg, unk
    Administration route: Oral
    Start date: 2009-09-02
    End date: 2009-09-13

Prograf
    Dosage: 4.7 mg, daily
    Administration route: Oral
    Start date: 2010-01-04
    End date: 2010-01-21

Prograf
    Dosage: 5 mg, unk
    Administration route: Oral
    Indication: Heart Transplant
    Start date: 2009-07-18
    End date: 2009-07-21

Prograf
    Dosage: 4.4 mg, unk
    Administration route: Oral
    Start date: 2009-07-23
    End date: 2009-08-09

Prograf
    Dosage: 5.7 mg, unk
    Administration route: Oral
    Start date: 2009-09-21
    End date: 2009-09-21

Prograf
    Dosage: 6.4 mg, unk
    Administration route: Oral
    Start date: 2009-10-05
    End date: 2009-10-21

Prograf
    Dosage: 6.4 mg, daily
    Administration route: Oral
    Start date: 2009-11-09

Prograf
    Dosage: 5.8 mg, unk
    Administration route: Oral
    Start date: 2010-04-09

Prograf
    Dosage: 4.9 mg, unk
    Administration route: Oral
    Start date: 2009-09-16
    End date: 2009-09-16

Prograf
    Dosage: 6.7 mg, unk
    Administration route: Oral
    Start date: 2009-10-22
    End date: 2009-11-08

Prograf
    Dosage: 5.4 mg, unk
    Administration route: Oral
    Start date: 2010-06-21
    End date: 2010-07-11

Prograf
    Dosage: 5.2 mg, unk
    Start date: 2010-07-12

Prograf
    Dosage: 7.7 mg, daily

Prograf
    Dosage: 4.7 mg, unk
    Administration route: Oral
    Start date: 2009-07-22
    End date: 2009-07-22

Prograf
    Dosage: 2.47 mg, unk
    Administration route: Oral
    Start date: 2009-09-14
    End date: 2009-09-14

Prograf
    Dosage: 4.4 mg, unk
    Administration route: Oral
    Start date: 2009-09-15
    End date: 2009-09-15

Prograf
    Dosage: 5 mg, unk
    Administration route: Oral
    Start date: 2010-04-07

Other drugs received by patient: Risperdal; Lipitor; Diflucan; Rocephin; Amaryl; Trazodone Hydrochloride; Clonazepam; Risperdal; Trazodone Hydrochloride; Diflucan; Haloperidol; Maglax; Sulperazon; Novolin R; Clindamycin Phosphate; Risperdal; DAI-Kenchu; Primobolan-Depot INJ; Amlodipine; Haloperidol; Cefazolin Sodium; Bisoprolol Fumarate; Glimicron; Acyclovir; Laxatives; Risperdal; Vancomycin Hydrochloride; Sulfamethoxazole and Trimethoprim; Risperdal; Vfend; Dogmatyl; Cellcept



Possible Prednisolone side effects in 73 year old female

Reported by a physician from Japan on 2012-07-13

Patient: 73 year old female, weighing 49.4 kg (108.7 pounds)

Reactions: Pain in Extremity, Grip Strength Decreased, Pain, Herpes Zoster

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Humira
    Indication: Rheumatoid Arthritis
    Start date: 2010-06-08
    End date: 2012-05-01

Prednisolone
    Dosage: 6 mg daily
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication
    Start date: 2009-05-12

Prograf
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-01-23

Rheumatrex
    Dosage: twice a week (4 mg, 2 mg)
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication
    Start date: 2009-05-12
    End date: 2010-10-05

Other drugs received by patient: Bucillamine; Lansoprazole; Celecoxib; Methotrexate; Methotrexate; Bucillamine; Folic Acid; Methotrexate; Sodium Risedronate Hydrate; Methotrexate; Methotrexate



Possible Prednisolone side effects in 73 year old female

Reported by a physician from Japan on 2012-07-12

Patient: 73 year old female, weighing 49.4 kg (108.7 pounds)

Reactions: Pain in Extremity, Pain, Grip Strength Decreased, Herpes Zoster

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Humira
    Indication: Rheumatoid Arthritis
    Start date: 2010-06-08
    End date: 2012-05-01

Prednisolone
    Dosage: 6 mg daily
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication
    Start date: 2009-05-12

Prograf
    Indication: Product Used FOR Unknown Indication

Rheumatrex
    Dosage: twice a week (4 mg, 2 mg)
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication
    Start date: 2009-05-12
    End date: 2010-10-05

Other drugs received by patient: Celecoxib; Tacrolimus; Folic Acid; Sodium Risedronate Hydrate; Methotrexate; Methotrexate; Lansoprazole; Methotrexate; Methotrexate; Bucillamine; Bucillamine; Methotrexate



Possible Prednisolone side effects in female

Reported by a health professional (non-physician/pharmacist) from Japan on 2012-07-10

Patient: female, weighing 51.0 kg (112.2 pounds)

Reactions: Cholecystitis Acute, Pyrexia, Herpes Zoster

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Inc424
    Dosage: unk
    Administration route: Oral
    Start date: 2012-04-02
    End date: 2012-04-09

Inc424
    Dosage: 30 mg, bid
    Administration route: Oral
    Indication: Myelofibrosis
    Start date: 2011-12-12
    End date: 2012-03-31

Inc424
    Dosage: 20 mg, qd
    Start date: 2012-05-25

Prednisolone
    Dosage: 10 mg, qd
    Administration route: Oral
    Indication: Platelet Count Decreased
    Start date: 2004-05-18

Other drugs received by patient: Lansoprazole; Celecoxib; Lasix; Vitamin B12; Magnesium Oxide; Exjade; Morphine; MS Contin; Halcion



Possible Prednisolone side effects in 73 year old female

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

Patient: 73 year old female, weighing 49.4 kg (108.7 pounds)

Reactions: Pain in Extremity, Pain, Grip Strength Decreased, Herpes Zoster

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Humira
    Indication: Rheumatoid Arthritis
    Start date: 2010-06-08
    End date: 2012-05-01

Prednisolone
    Dosage: 6 mg daily
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication
    Start date: 2009-05-12

Prograf
    Indication: Product Used FOR Unknown Indication

Rheumatrex
    Dosage: twice a week (4 mg, 2 mg)
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication
    Start date: 2009-05-12
    End date: 2010-10-05

Other drugs received by patient: Methotrexate; Methotrexate; Bucillamine; Celecoxib; Methotrexate; Bucillamine; Sodium Risedronate Hydrate; Methotrexate; Lansoprazole; Folic Acid



Possible Prednisolone side effects in 66 year old female

Reported by a physician from Korea, Republic of on 2012-06-27

Patient: 66 year old female

Reactions: Encephalitis Post Varicella, Angiopathy, Herpes Zoster

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Adalimumab
    Indication: Rheumatoid Arthritis

Adalimumab

Methotrexate
    Dosage: 17.5 mg per week
    Indication: Product Used FOR Unknown Indication

Prednisolone
    Dosage: 10 mg daily
    Indication: Product Used FOR Unknown Indication



Possible Prednisolone side effects in 44 year old male

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

Patient: 44 year old male, weighing 130.0 kg (286.0 pounds)

Reactions: Pancreatitis, Herpes Zoster

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Actemra
    Dosage: last dose prior to sae: 24/apr/2012
    Indication: Rheumatoid Arthritis
    Start date: 2012-03-27

Prednisolone
    Administration route: Oral
    Indication: Rheumatoid Arthritis

Other drugs received by patient: Candesartan; Pantoprazole



Possible Prednisolone side effects in female

Reported by a physician from Japan on 2012-06-18

Patient: female, weighing 51.0 kg (112.2 pounds)

Reactions: Cholecystitis Acute, Pyrexia, Herpes Zoster

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Inc424
    Dosage: 20 mg, qd
    Start date: 2012-05-25

Inc424
    Dosage: 30 mg, bid
    Administration route: Oral
    Indication: Myelofibrosis
    Start date: 2011-12-12
    End date: 2012-03-31

Inc424
    Dosage: unk
    Administration route: Oral
    Start date: 2012-04-02
    End date: 2012-04-09

Prednisolone
    Dosage: 10 mg, qd
    Administration route: Oral
    Indication: Platelet Count Decreased
    Start date: 2004-05-18

Other drugs received by patient: Lansoprazole; MS Contin; Exjade; Magnesium Oxide; Vitamin B12; Celecoxib; Lasix; Morphine; Halcion



Possible Prednisolone side effects in 73 year old female

Reported by a physician from Japan on 2012-06-18

Patient: 73 year old female, weighing 49.4 kg (108.7 pounds)

Reactions: Pain in Extremity, Grip Strength Decreased, Herpes Zoster

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Humira
    Indication: Rheumatoid Arthritis
    Start date: 2010-06-08
    End date: 2012-05-01

Prednisolone
    Dosage: 6 mg daily
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication
    Start date: 2009-05-12

Prograf
    Indication: Product Used FOR Unknown Indication

Rheumatrex
    Dosage: twice a week (4 mg, 2 mg)
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication
    Start date: 2009-05-12
    End date: 2010-10-05

Other drugs received by patient: Methotrexate; Lansoprazole; Folic Acid; Celecoxib; Bucillamine; Methotrexate; Bucillamine; Sodium Risedronate Hydrate; Methotrexate; Methotrexate



Possible Prednisolone side effects in male

Reported by a physician from Japan on 2012-06-08

Patient: male, weighing 67.0 kg (147.4 pounds)

Reactions: Pneumonia Aspiration, Diabetes Mellitus, Ileus, Aspergillosis Oral, Platelet Count Decreased, Altered State of Consciousness, Herpes Zoster

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Akineton
    Dosage: 3 mg, unk
    Administration route: Oral
    Start date: 2008-08-14
    End date: 2009-08-24

Akineton
    Dosage: 3 mg, unk
    Administration route: Oral
    Start date: 2009-08-31
    End date: 2009-09-01

Certican
    Dosage: 0.75 mg, unk
    Administration route: Oral
    Start date: 2009-08-10

Certican
    Dosage: 0.5 mg, unk
    Administration route: Oral
    Start date: 2009-10-14
    End date: 2009-10-14

Certican
    Dosage: 1 mg, unk
    Administration route: Oral
    Start date: 2010-02-20
    End date: 2010-03-08

Certican
    Dosage: 0.5 mg, unk
    Administration route: Oral
    Start date: 2009-08-08
    End date: 2009-08-09

Certican
    Dosage: 1.25 mg, unk
    Administration route: Oral
    Start date: 2009-08-25
    End date: 2009-08-26

Certican
    Dosage: 1 mg, unk
    Administration route: Oral
    Start date: 2009-08-07
    End date: 2009-08-07

Certican
    Dosage: 1 mg, unk
    Administration route: Oral
    Start date: 2009-10-15
    End date: 2009-10-15

Certican
    Dosage: 0.5 mg, unk
    Administration route: Oral
    Start date: 2009-10-16
    End date: 2009-10-16

Certican
    Dosage: 1 mg, unk
    Administration route: Oral
    Start date: 2009-08-12
    End date: 2009-08-24

Certican
    Dosage: 0.75 mg, unk
    Administration route: Oral
    Start date: 2010-03-09
    End date: 2010-03-15

Certican
    Dosage: 1.5 mg, unk
    Indication: Heart Transplant
    Start date: 2009-07-30
    End date: 2009-08-06

Certican
    Dosage: 1 mg, unk
    Administration route: Oral
    Start date: 2009-08-27
    End date: 2009-09-01

Certican
    Dosage: 0.5 mg, unk
    Administration route: Oral
    Start date: 2010-03-16
    End date: 2010-04-15

Certican
    Dosage: 0.75 mg, unk
    Administration route: Oral
    Start date: 2010-04-16

Clonazepam

Meropenem
    Dosage: 1.5 mg, unk
    Start date: 2009-08-11
    End date: 2009-08-24

Meropenem
    Dosage: unk ukn, unk

Meropenem
    Dosage: 1.5 mg, unk
    Start date: 2009-08-31
    End date: 2009-09-09

Prednisolone
    Dosage: 2.5 mg, unk
    Administration route: Oral
    Indication: Heart Transplant
    Start date: 2009-01-06
    End date: 2009-09-02

Prednisolone
    Dosage: unk ukn, unk
    Administration route: Oral
    Start date: 2010-05-28

Prednisolone
    Dosage: 10 mg, unk
    Administration route: Oral
    Start date: 2009-09-03
    End date: 2010-03-26

Prednisolone
    Dosage: 7.5 mg, unk
    Administration route: Oral
    Start date: 2010-03-27
    End date: 2010-04-01

Prednisolone
    Dosage: 5 mg, unk
    Administration route: Oral
    Start date: 2010-04-24
    End date: 2010-05-01

Prograf
    Dosage: 4.7 mg, unk
    Administration route: Oral
    Start date: 2009-07-22
    End date: 2009-07-22

Prograf
    Dosage: 4.9 mg, unk
    Administration route: Oral
    Start date: 2009-09-16
    End date: 2009-09-16

Prograf
    Dosage: 6 mg, unk
    Administration route: Oral
    Start date: 2009-09-22
    End date: 2009-09-24

Prograf
    Dosage: 5.8 mg, unk
    Administration route: Oral
    Start date: 2010-03-26
    End date: 2010-03-27

Prograf
    Dosage: 4 mg, unk
    Administration route: Oral
    Start date: 2009-08-15
    End date: 2009-08-16

Prograf
    Dosage: 6.7 mg, unk
    Administration route: Oral
    Start date: 2009-10-22
    End date: 2009-11-08

Prograf
    Dosage: 6.4 mg, daily
    Administration route: Oral
    Start date: 2009-11-09

Prograf
    Dosage: 4.7 mg, daily
    Administration route: Oral
    Start date: 2010-01-04
    End date: 2010-01-21

Prograf
    Dosage: 5.8 mg, unk
    Administration route: Oral
    Start date: 2010-04-09

Prograf
    Dosage: 5 mg, unk
    Administration route: Oral
    Indication: Heart Transplant
    Start date: 2009-07-18
    End date: 2009-07-21

Prograf
    Dosage: 4.2 mg, unk
    Administration route: Oral
    Start date: 2009-08-10
    End date: 2009-08-14

Prograf
    Dosage: 5.4 mg, unk
    Administration route: Oral
    Start date: 2009-09-17
    End date: 2009-09-20

Prograf
    Dosage: 6.4 mg, unk
    Administration route: Oral
    Start date: 2009-10-05
    End date: 2009-10-21

Prograf
    Dosage: 4.4 mg, unk
    Administration route: Oral
    Start date: 2009-07-23
    End date: 2009-08-09

Prograf
    Dosage: 5 mg, unk
    Administration route: Oral
    Start date: 2009-09-02
    End date: 2009-09-13

Prograf
    Dosage: 2.47 mg, unk
    Administration route: Oral
    Start date: 2009-09-14
    End date: 2009-09-14

Prograf
    Dosage: 6.5 mg, unk
    Administration route: Oral
    Start date: 2009-09-25
    End date: 2009-10-01

Prograf
    Dosage: 5.4 mg, unk
    Administration route: Oral
    Start date: 2010-06-21
    End date: 2010-07-11

Prograf
    Dosage: 7.7 mg, daily

Prograf
    Dosage: 6.4 mg, daily

Prograf
    Dosage: 3.7 mg, unk
    Administration route: Oral
    Start date: 2009-08-17
    End date: 2009-09-01

Prograf
    Dosage: 6 mg, unk
    Administration route: Oral
    Start date: 2010-05-26
    End date: 2010-06-20

Prograf
    Dosage: 5.2 mg, unk
    Start date: 2010-07-12

Prograf
    Dosage: 4.4 mg, unk
    Administration route: Oral
    Start date: 2009-09-15
    End date: 2009-09-15

Prograf
    Dosage: 5.7 mg, unk
    Administration route: Oral
    Start date: 2009-09-21
    End date: 2009-09-21

Prograf
    Dosage: 6.2 mg, unk
    Administration route: Oral
    Start date: 2009-10-02
    End date: 2009-10-04

Prograf
    Dosage: 7 mg, daily
    Administration route: Oral
    Start date: 2009-12-16

Prograf
    Dosage: 6.4 mg, unk
    Administration route: Oral
    Start date: 2010-01-22
    End date: 2010-01-27

Prograf
    Dosage: 4.7 mg, unk
    Administration route: Oral
    Start date: 2010-01-28
    End date: 2010-02-15

Prograf
    Dosage: 5.6 mg, unk
    Administration route: Oral
    Start date: 2010-02-16
    End date: 2010-03-25

Prograf
    Dosage: 6 mg, unk
    Administration route: Oral
    Start date: 2010-03-28
    End date: 2010-04-06

Prograf
    Dosage: 5 mg, unk
    Administration route: Oral
    Start date: 2010-04-07

Other drugs received by patient: Diflucan; Amaryl; Cellcept; Risperdal; Risperdal; Novolin R; Risperdal; Bisoprolol Fumarate; Amlodipine; Clindamycin Phosphate; Glimicron; Rocephin; Cefoperazone Sodium; Vfend; Risperdal; Trazodone Hydrochloride; Trazodone Hydrochloride; Dogmatyl; DAI-Kenchu; Clonazepam; Acyclovir; Risperdal; Haloperidol; Haloperidol; Cefazolin Sodium; Vancomycin Hydrochloride; Maglax; Primobolan-Depot INJ; Lipitor; Diflucan



Possible Prednisolone side effects in female

Reported by a physician from Japan on 2012-06-08

Patient: female, weighing 41.0 kg (90.2 pounds)

Reactions: Herpes Zoster

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Methotrexate
    Administration route: Oral
    Start date: 2012-01-11
    End date: 2012-02-03

Methotrexate
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    Start date: 2012-02-08
    End date: 2012-02-24

Methotrexate
    Administration route: Oral
    Start date: 2012-03-08

Prednisolone
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication

Simponi
    Indication: Rheumatoid Arthritis
    Start date: 2012-02-08

Simponi
    Start date: 2012-01-11



Possible Prednisolone side effects in female

Reported by a health professional (non-physician/pharmacist) from Japan on 2012-06-04

Patient: female, weighing 51.0 kg (112.2 pounds)

Reactions: Dysstasia, Cholecystitis Acute, Arthralgia, Pyrexia, Herpes Zoster

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Inc424
    Dosage: unk
    Administration route: Oral
    Start date: 2012-04-02
    End date: 2012-04-09

Inc424
    Dosage: 30 mg, bid
    Administration route: Oral
    Indication: Myelofibrosis
    Start date: 2011-12-12
    End date: 2012-03-31

Prednisolone
    Dosage: 10 mg, qd
    Administration route: Oral
    Indication: Platelet Count Decreased
    Start date: 2004-05-18

Other drugs received by patient: Vitamin B12; Celecoxib; Halcion; Magnesium Oxide; Morphine; Exjade; MS Contin; Lansoprazole; Lasix



Possible Prednisolone side effects in female

Reported by a physician from Japan on 2012-05-31

Patient: female, weighing 41.0 kg (90.2 pounds)

Reactions: Herpes Zoster

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Methotrexate
    Administration route: Oral
    Start date: 2012-01-11
    End date: 2012-02-03

Methotrexate
    Administration route: Oral
    Start date: 2012-03-08

Methotrexate
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    Start date: 2012-02-08
    End date: 2012-02-24

Prednisolone
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication

Simponi
    Indication: Rheumatoid Arthritis
    Start date: 2012-02-08

Simponi
    Start date: 2012-01-11



Possible Prednisolone side effects in female

Reported by a physician from Japan on 2012-05-29

Patient: female, weighing 51.0 kg (112.2 pounds)

Reactions: Cholecystitis Acute, Pyrexia, Herpes Zoster

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Inc424
    Dosage: 30 mg, bid
    Administration route: Oral
    Indication: Myelofibrosis
    Start date: 2011-12-12
    End date: 2012-03-31

Prednisolone
    Dosage: 10 mg, qd
    Administration route: Oral
    Indication: Platelet Count Decreased
    Start date: 2004-05-18

Other drugs received by patient: Lansoprazole; Exjade; Lasix; Halcion; Vitamin B12; MS Contin; Morphine; Magnesium Oxide



Possible Prednisolone side effects in 60 year old female

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

Patient: 60 year old female, weighing 52.0 kg (114.4 pounds)

Reactions: Herpes Zoster

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Prednisolone
    Administration route: Oral
    Start date: 2011-08-01
    End date: 2011-08-10

Prednisolone
    Administration route: Oral
    Start date: 2011-09-07
    End date: 2011-09-20

Prednisolone
    Administration route: Oral
    Start date: 2011-08-11
    End date: 2011-08-24

Prednisolone
    Administration route: Oral
    Start date: 2011-08-25
    End date: 2011-09-06

Prednisolone
    Administration route: Oral
    Indication: Colitis Ulcerative
    Start date: 2011-07-14
    End date: 2011-07-31

Prednisolone
    Administration route: Oral
    Start date: 2011-06-20
    End date: 2011-07-13

Prednisolone
    Administration route: Oral
    Start date: 2011-09-21
    End date: 2011-10-05

Prednisolone
    Administration route: Oral
    Start date: 2011-05-28
    End date: 2011-06-19

Remicade
    Start date: 2011-07-14

Remicade
    Start date: 2011-10-06

Remicade
    Dosage: third dose
    Indication: Colitis Ulcerative
    Start date: 2011-08-11

Remicade
    Dosage: 4th dose
    Start date: 2011-08-25

Remicade
    Dosage: first dose
    Start date: 2011-06-30

Other drugs received by patient: Asacol; Ferrum; Miya BM



Possible Prednisolone side effects in 44 year old male

Reported by a individual with unspecified qualification from Germany on 2012-05-15

Patient: 44 year old male, weighing 130.0 kg (286.0 pounds)

Reactions: Pancreatitis, Herpes Zoster

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Actemra
    Dosage: last dose prior to sae: 24/apr/2012
    Indication: Rheumatoid Arthritis
    Start date: 2012-03-27

Prednisolone
    Administration route: Oral
    Indication: Rheumatoid Arthritis

Other drugs received by patient: Candesartan Cilexetil; Pantoprazole



Possible Prednisolone side effects in 77 year old female

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

Patient: 77 year old female, weighing 36.0 kg (79.2 pounds)

Reactions: Blood Alkaline Phosphatase Increased, Back Pain, Blood Urea Increased, Pneumonia, Urinary Tract Infection, Pubis Fracture, General Physical Health Deterioration, Herpes Zoster, Renal Impairment, Sepsis, Dehydration, Neutropenia, Thrombocytopenia, Blood Creatinine Increased

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Exjade
    Dosage: 750 mg, qd
    Administration route: Oral
    Indication: Myelodysplastic Syndrome
    Start date: 2009-09-16
    End date: 2011-04-03

Exjade
    Dosage: 625 mg, qd
    Administration route: Oral
    Start date: 2011-05-07
    End date: 2011-05-22

Exjade
    Dosage: 625 mg, every other day
    Administration route: Oral
    Start date: 2011-05-23

Prednisolone
    Dosage: 6 mg, daily
    Administration route: Oral
    Start date: 2010-02-03
    End date: 2010-04-21

Prednisolone
    Dosage: 8 mg, daily
    Administration route: Oral
    End date: 2009-09-29

Prednisolone
    Dosage: 5 mg daily
    Administration route: Oral
    Start date: 2010-04-22

Prednisolone
    Dosage: 7 mg, daily
    Administration route: Oral
    Start date: 2009-09-30
    End date: 2010-02-02

Revlimid
    Dosage: 5 mg, daily
    Administration route: Oral
    Indication: Myelodysplastic Syndrome
    Start date: 2011-04-12
    End date: 2011-05-02

Revlimid
    Dosage: 5 mg, daily
    Administration route: Oral
    Start date: 2011-05-19
    End date: 2011-06-01

Other drugs received by patient: Amaryl; Timoptol-XE; RED Blood Cells, Concentrated; Novolin R; Voglibose; Azopt; Famotidine; Novolin R; Xalatan; Novolin R; RED Blood Cells, Concentrated; Alendronate Sodium; Clarithromycin; Glufast; Mucodyne; Equa; Platelets; Platelets; Desferal



Possible Prednisolone side effects in 77 year old female

Reported by a physician from Japan on 2012-05-14

Patient: 77 year old female, weighing 36.0 kg (79.2 pounds)

Reactions: Back Pain, Blood Alkaline Phosphatase Increased, Blood Urea Increased, Pneumonia, Pubis Fracture, Urinary Tract Infection, General Physical Health Deterioration, Herpes Zoster, Renal Impairment, Dehydration, Sepsis, Neutropenia, Blood Creatinine Increased, Thrombocytopenia

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Exjade
    Dosage: 625 mg, qd
    Administration route: Oral
    Start date: 2011-05-07
    End date: 2011-05-22

Exjade
    Dosage: 625 mg, every other day
    Administration route: Oral
    Start date: 2011-05-23

Exjade
    Dosage: 750 mg, qd
    Administration route: Oral
    Indication: Myelodysplastic Syndrome
    Start date: 2009-09-16
    End date: 2011-04-03

Prednisolone
    Dosage: 8 mg, daily
    Administration route: Oral
    End date: 2009-09-29

Prednisolone
    Dosage: 6 mg, daily
    Administration route: Oral
    Start date: 2010-02-03
    End date: 2010-04-21

Prednisolone
    Dosage: 5 mg daily
    Administration route: Oral
    Start date: 2010-04-22

Prednisolone
    Dosage: 7 mg, daily
    Administration route: Oral
    Start date: 2009-09-30
    End date: 2010-02-02

Revlimid
    Dosage: 5 mg, daily
    Administration route: Oral
    Start date: 2011-05-19
    End date: 2011-06-01

Revlimid
    Dosage: 5 mg, daily
    Administration route: Oral
    Indication: Myelodysplastic Syndrome
    Start date: 2011-04-12
    End date: 2011-05-02

Other drugs received by patient: RED Blood Cells, Concentrated; Alendronate Sodium; Xalatan; Platelets; Novolin R; Timoptol-XE; Equa; Novolin R; Glufast; Clarithromycin; Voglibose; Platelets; Famotidine; RED Blood Cells, Concentrated; Novolin R; Desferal; Amaryl; Mucodyne; Azopt



Possible Prednisolone side effects in 55 year old female

Reported by a physician from Japan on 2012-05-03

Patient: 55 year old female, weighing 55.0 kg (121.0 pounds)

Reactions: Blood Urea Increased, Glycosylated Haemoglobin Increased, Herpes Zoster

Drug(s) suspected as cause:
Prednisolone
    Dosage: 7.5; 7;6;5 mg, unknown/d, oral
    Administration route: Oral
    Start date: 2007-11-13
    End date: 2008-03-24

Prednisolone
    Dosage: 7.5; 7;6;5 mg, unknown/d, oral
    Administration route: Oral
    Start date: 2008-03-25
    End date: 2008-07-22

Prednisolone
    Dosage: 7.5; 7;6;5 mg, unknown/d, oral
    Administration route: Oral
    End date: 2007-11-12

Prednisolone
    Dosage: 7.5; 7;6;5 mg, unknown/d, oral
    Administration route: Oral
    Start date: 2008-07-23

Tacrolimus
    Dosage: 3;1;1.5;1 mg, unknown.d, oral
    Administration route: Oral
    Indication: Lupus Nephritis
    Start date: 2007-08-17
    End date: 2007-12-24

Tacrolimus
    Dosage: 3;1;1.5;1 mg, unknown.d, oral
    Administration route: Oral
    Indication: Lupus Nephritis
    Start date: 2007-12-25

Tacrolimus
    Dosage: 3;1;1.5;1 mg, unknown.d, oral
    Administration route: Oral
    Indication: Lupus Nephritis
    Start date: 2007-05-11
    End date: 2007-08-16

Other drugs received by patient: Livalo; Enalapril Maleate; Allopurinol; Amoban (Zopiclone); Nesina (Alogliptin Benzoate); Rohypnol (Flunitrazepam); Carvedilol; Adalat; Rabeprazole Sodium; Nesina (Alogliptin Benzoate)



Possible Prednisolone side effects in female

Reported by a physician from Japan on 2012-04-17

Patient: female, weighing 51.0 kg (112.2 pounds)

Reactions: Cholecystitis Acute, Herpes Zoster

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Inc424
    Dosage: unk
    Administration route: Oral
    Indication: Myelofibrosis
    Start date: 2011-12-12
    End date: 2012-03-31

Prednisolone
    Dosage: 10 mg, unk
    Administration route: Oral
    Indication: Platelet Count Decreased
    Start date: 2004-05-18

Other drugs received by patient: Lasix; Morphine; Exjade; Lansoprazole; Magnesium Oxide; Halcion; Vitamin B12; MS Contin



Possible Prednisolone side effects in female

Reported by a physician from Japan on 2012-04-11

Patient: female, weighing 41.0 kg (90.2 pounds)

Reactions: Herpes Zoster

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Methotrexate
    Indication: Rheumatoid Arthritis
    Start date: 2012-02-09

Methotrexate
    Start date: 2012-01-12

Prednisolone
    Indication: Product Used FOR Unknown Indication

Simponi
    Indication: Rheumatoid Arthritis
    Start date: 2012-02-08

Simponi
    Start date: 2012-01-12



Possible Prednisolone side effects in 60 year old female

Reported by a physician from Japan on 2012-04-06

Patient: 60 year old female, weighing 52.0 kg (114.4 pounds)

Reactions: Herpes Zoster

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Prednisolone
    Administration route: Oral
    Indication: Colitis Ulcerative
    Start date: 2011-08-11
    End date: 2011-08-24

Prednisolone
    Administration route: Oral
    Start date: 2011-06-20
    End date: 2011-07-13

Prednisolone
    Administration route: Oral
    Start date: 2011-09-21
    End date: 2011-10-05

Prednisolone
    Administration route: Oral
    Start date: 2011-09-07
    End date: 2011-09-20

Prednisolone
    Administration route: Oral
    Start date: 2011-05-28
    End date: 2011-06-19

Prednisolone
    Administration route: Oral
    Start date: 2011-08-25
    End date: 2011-09-06

Prednisolone
    Administration route: Oral
    Start date: 2011-08-01
    End date: 2011-08-10

Prednisolone
    Administration route: Oral
    Start date: 2011-07-14
    End date: 2011-07-31

Remicade
    Dosage: first dose
    Start date: 2011-06-30

Remicade
    Dosage: third dose
    Start date: 2011-08-11

Remicade
    Indication: Colitis Ulcerative
    Start date: 2011-10-06

Remicade
    Start date: 2011-07-14

Remicade
    Dosage: 4th dose
    Start date: 2011-08-25

Other drugs received by patient: Ferrum; Asacol; Miya BM



Possible Prednisolone side effects in male

Reported by a physician from Japan on 2012-03-30

Patient: male, weighing 60.0 kg (132.0 pounds)

Reactions: Oral Candidiasis, Anal Abscess, Device Related Infection, Herpes Zoster

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Mercaptopurine
    Administration route: Oral
    Indication: Colitis Ulcerative

Prednisolone
    Administration route: Oral
    Indication: Colitis Ulcerative

Remicade
    Start date: 2011-12-12

Remicade
    Start date: 2011-06-21

Remicade
    Start date: 2011-08-22

Remicade
    Start date: 2011-07-04

Remicade
    Indication: Colitis Ulcerative
    Start date: 2012-02-06

Remicade
    Start date: 2011-10-17

Other drugs received by patient: Zolpidem; Pentasa; Famotidine; Warfarin Sodium; Tegretol; Miya BM; Actonel



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