Common Predonine Side Effects


The most commonly reported Predonine side effects (click to view or check a box to report):

Blood Creatinine Increased (13)
Cerebral Infarction (12)
Grip Strength Decreased (10)
Dysarthria (10)
Leukoaraiosis (9)
Jc Virus Infection (9)
C-reactive Protein Increased (8)
Interstitial Lung Disease (8)
White Blood Cell Count Decreased (7)
Pancytopenia (7)
Osteomyelitis (6)
Blood Urea Increased (6)
Pneumonia (6)
Platelet Count Decreased (6)
Progressive Multifocal Leukoencephalopathy (6)
Sepsis (6)
Respiratory Failure (6)
Hepatic Function Abnormal (5)
Renal Impairment (5)
Herpes Zoster (5)

➢ More



If you or someone in your family has experienced a serious side effect to a health product, you are encouraged to report the experience to your health care professional (e.g. physician, pharmacist). You could also complete a copy of the side effect reporting form or report your side effect to FDA.

Predonine Side Effects Reported to FDA



Predonine Side Effect Report#8097914
Pneumonia Bacterial, Endocarditis, Sepsis, Abscess Limb, Skin Ulcer, Arthritis Bacterial, Cerebral Infarction, Platelet Count Decreased, Red Blood Cell Count Decreased
This is a report of a 55-year-old female patient (weight: NA) from Country Not Specified, suffering from the following health symptoms/conditions: rheumatoid arthritis, who was treated with Predonine (dosage: NA, start time:
Mar 24, 2009), combined with: NA. and developed a serious reaction and side effect(s): Pneumonia Bacterial, Endocarditis, Sepsis, Abscess Limb, Skin Ulcer, Arthritis Bacterial, Cerebral Infarction, Platelet Count Decreased, Red Blood Cell Count Decreased after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Predonine treatment in female patients, resulting in Pneumonia Bacterial side effect. The patient was hospitalized.
Predonine Side Effect Report#7746122-9
Speech Disorder, Hallucination, Influenza, Upper Respiratory Tract Infection, Restlessness, Psychotic Disorder, Delusion, Diabetes Mellitus, Nasopharyngitis
This report suggests a potential Predonine (prednisolone) Per Oral Nos Speech Disorder side effect(s) that can have serious consequences. A 43-year-old male patient (weight: NA) from Japan was diagnosed with the following symptoms/conditions: lupus nephritis and used Predonine (prednisolone) Per Oral Nos (dosage: 17.5 Mg, Oral 15 Mg, Oral 14 Mg, Oral) starting
Aug 20, 2008. After starting Predonine (prednisolone) Per Oral Nos the patient began experiencing various side effects, including: Speech Disorder, Hallucination, Influenza, Upper Respiratory Tract Infection, Restlessness, Psychotic Disorder, Delusion, Diabetes Mellitus, NasopharyngitisAdditional drugs used concurrently: NA. Although Predonine (prednisolone) Per Oral Nos demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Speech Disorder, may still occur.
Predonine Side Effect Report#7460434-8
Mucous Membrane Disorder, C-reactive Protein Increased, Aspartate Aminotransferase Increased, Alanine Aminotransferase Increased, Thrombotic Microangiopathy, Acute Graft Versus Host Disease, Pancytopenia, Pyrexia, Leukoencephalopathy
This Mucous Membrane Disorder problem was reported by a physician from Japan. A male patient (weight: NA) was diagnosed with the following symptoms/conditions: immunosuppression. On
Jul 22, 2005 this consumer started treatment with Predonine (dosage: 2mgk Per Day). The following drugs were being taken at the same time:
  • Methotrexate (10mgm2 Per Day)
  • Solu-cortef (50mg Per Day)
  • Vicclox (250mg Per Day)
  • Cyclosporine (3mgk Per Day)
  • Firstcin (3g Per Day)
  • Kytril (2mg Per Day)
  • Furosemide (40mg Per Day)
  • Alkeran (180mgm2 Per Day)
When using Predonine, the patient experienced the following unwanted symptoms/side effects: Mucous Membrane Disorder, C-reactive Protein Increased, Aspartate Aminotransferase Increased, Alanine Aminotransferase Increased, Thrombotic Microangiopathy, Acute Graft Versus Host Disease, Pancytopenia, Pyrexia, LeukoencephalopathyAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Mucous Membrane Disorder, may become evident only after a product is in use by the general population.
Predonine Side Effect Report#7458451-7
Pancreatitis Acute, Hepatic Failure, Respiratory Failure, Epstein-barr Virus Infection
This Pancreatitis Acute side effect was reported by a physician from Japan. A female patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Predonine (drug dosage: 60mg Per Day), which was initiated on
Feb 02, 2008. Concurrently used drugs:
  • Gaster (30mg Per Day)
  • Alkeran (70mg Per Day)
  • Fludara (30mgm2 Per Day)
  • Furosemide (30mg Per Day)
  • Kytril
  • Nafamostat (400mg Per Day)
  • Meropenem (.5g Per Day)
  • Cyclosporine (20mg Per Day)
.After starting to take Predonine the consumer reported adverse symptoms, such as: Pancreatitis Acute, Hepatic Failure, Respiratory Failure, Epstein-barr Virus InfectionThese side effects may potentially be related to Predonine.
Predonine Side Effect Report#7457529-1
Respiratory Failure, Pneumonia, Pneumothorax, Bronchopulmonary Aspergillosis, Haemorrhage, Fall, Interstitial Lung Disease, Rib Fracture
This is a report of a 77-year-old female patient (weight: NA) from Japan, suffering from the following health symptoms/conditions: rheumatoid arthritis, who was treated with Predonine (dosage: Dose Unit:1 Tabs Dose Increased To 30mg/kg, start time:
Aug 19, 2008), combined with:
  • Kentan
  • Lansoprazole
  • Amaryl
  • Orencia (On 1nov10 Received Every 4wks 25oct10:250mg 8nov10:500mg 22nov10:500mg 21dec10:500mg)
  • Prograf
  • Rebamipide
  • Itraconazole
  • Isoniazid
and developed a serious reaction and side effect(s): Respiratory Failure, Pneumonia, Pneumothorax, Bronchopulmonary Aspergillosis, Haemorrhage, Fall, Interstitial Lung Disease, Rib Fracture after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Predonine treatment in female patients, resulting in Respiratory Failure side effect. The patient was hospitalized.
Predonine Side Effect Report#7455770-5
Interstitial Lung Disease
This report suggests a potential Predonine Interstitial Lung Disease side effect(s) that can have serious consequences. A 78-year-old male patient (weight: NA) from Japan was diagnosed with the following symptoms/conditions: interstitial lung disease,metastatic renal cell carcinoma,hypertension and used Predonine (dosage: 5 Mg, 1x/day) starting
Apr 01, 2010. After starting Predonine the patient began experiencing various side effects, including: Interstitial Lung DiseaseAdditional drugs used concurrently:
  • Sutent (25 Mg, 1x/day)
  • Baylotensin (10 Mg, 1x/day)
Although Predonine demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Interstitial Lung Disease, may still occur.
Predonine Side Effect Report#7455764-X
Pneumonia, Ureteric Stenosis, Urinary Tract Infection, Renal Pelvis Fistula, Lymphocele
This Pneumonia problem was reported by a physician from Japan. A 68-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On
Oct 30, 2009 this consumer started treatment with Predonine (dosage: 30 Mg). The following drugs were being taken at the same time: NA. When using Predonine, the patient experienced the following unwanted symptoms/side effects: Pneumonia, Ureteric Stenosis, Urinary Tract Infection, Renal Pelvis Fistula, LymphoceleThe patient was hospitalized.Although all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Pneumonia, may become evident only after a product is in use by the general population.
Predonine Side Effect Report#7446560-8
Femur Fracture
This Femur Fracture side effect was reported by a physician from Japan. A 63-year-old female patient (weight:NA) experienced the following symptoms/conditions: rheumatoid arthritis.The patient was prescribed Predonine (drug dosage: NA), which was initiated on
Jan 01, 2003. Concurrently used drugs:
  • Mucodyne
  • Seltouch
  • Nobfen (loxoprofen Sodium)
  • Lac-b
  • Fosamax
  • Calblock
  • Cytotec
  • Fosamax
.After starting to take Predonine the consumer reported adverse symptoms, such as: Femur FractureThese side effects may potentially be related to Predonine. The patient was hospitalized.
Predonine Side Effect Report#7443203-4
Arterial Occlusive Disease
This is a report of a male patient (weight: NA) from Japan, suffering from the following health symptoms/conditions: NA, who was treated with Predonine (dosage: 2.5mg Per Day, start time:
Feb 21, 2011), combined with:
  • Aspirin (100mg Per Day)
  • Takepron (30mg Per Day)
and developed a serious reaction and side effect(s): Arterial Occlusive Disease after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Predonine treatment in male patients, resulting in Arterial Occlusive Disease side effect.
Predonine Side Effect Report#7442119-7
Altered State Of Consciousness, Renal Impairment
This report suggests a potential Predonine Altered State Of Consciousness side effect(s) that can have serious consequences. A male patient (weight: NA) from Japan was diagnosed with the following symptoms/conditions: NA and used Predonine (dosage: 1 Df, Unk) starting
Jul 10, 2009. After starting Predonine the patient began experiencing various side effects, including: Altered State Of Consciousness, Renal ImpairmentAdditional drugs used concurrently:
  • Exjade (875 Mg/day)
  • Lasix (0.5 Df, Unk)
  • Urocalun (6 Df, Unk)
  • Atarax
  • Digosin (0.5 Df, Unk)
  • Exjade (250 Mg/day)
  • Rocaltrol (3 Df, Unk)
  • Livact (2 Df, Unk)
The patient was hospitalized. Although Predonine demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Altered State Of Consciousness, may still occur.
Predonine Side Effect Report#7438545-2
Muscular Weakness, Hypoaesthesia
This Muscular Weakness problem was reported by a physician from Japan. A 45-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On NS this consumer started treatment with Predonine (dosage: NA). The following drugs were being taken at the same time:
  • Remicade
When using Predonine, the patient experienced the following unwanted symptoms/side effects: Muscular Weakness, HypoaesthesiaThe patient was hospitalized.Although all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Muscular Weakness, may become evident only after a product is in use by the general population.
Predonine Side Effect Report#7433760-6
Skin Ulcer
This Skin Ulcer side effect was reported by a physician from Japan. A 49-year-old female patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Predonine /00016201/ (drug dosage: 0.5 Df, 1x/day), which was initiated on
May 01, 2010. Concurrently used drugs:
  • Rheumatrex (6 Mg, Weekly)
  • Enbrel (25 Mg, Weekly)
  • Azulfidine (500 Mg, 2x/day)
.After starting to take Predonine /00016201/ the consumer reported adverse symptoms, such as: Skin UlcerThese side effects may potentially be related to Predonine /00016201/. The patient was hospitalized.
Predonine Side Effect Report#7432635-6
Acute Respiratory Distress Syndrome, Pancreatitis Necrotising, Respiratory Failure, Bronchopneumonia
This is a report of a male patient (weight: NA) from Japan, suffering from the following health symptoms/conditions: NA, who was treated with Predonine (dosage: NA, start time:
Jan 01, 2009), combined with:
  • Ludiomil
  • Bactrim
  • Actemra (Administered 5 Times)
  • Alendronate Sodium
  • Paxil
and developed a serious reaction and side effect(s): Acute Respiratory Distress Syndrome, Pancreatitis Necrotising, Respiratory Failure, Bronchopneumonia after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Predonine treatment in male patients, resulting in Acute Respiratory Distress Syndrome side effect.
Predonine Side Effect Report#7430783-8
Breast Cancer
This report suggests a potential Predonine Breast Cancer side effect(s) that can have serious consequences. A 33-year-old female patient (weight: NA) from Japan was diagnosed with the following symptoms/conditions: asthma and used Predonine (dosage: NA) starting
Apr 05, 2010. After starting Predonine the patient began experiencing various side effects, including: Breast CancerAdditional drugs used concurrently:
  • Symbicort (2 Df Two Times A Day)
  • Lysozyme Hydrochloride
  • Chlorpheniramine Maleate
  • Symbicort (1 Df Two Times A Day)
  • Methylephedrine
  • Methylephedrine
  • Codeine
The patient was hospitalized. Although Predonine demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Breast Cancer, may still occur.
Predonine Side Effect Report#7429612-8
Arterial Occlusive Disease
This Arterial Occlusive Disease problem was reported by a physician from Japan. A male patient (weight: NA) was diagnosed with the following symptoms/conditions: idiopathic thrombocytopenic purpura. On
Mar 17, 2011 this consumer started treatment with Predonine (dosage: 5mg Per Day). The following drugs were being taken at the same time:
  • Sigmart (20mg Per Day)
  • Plavix (75mg Per Day)
  • Takepron (30mg Per Day)
  • Aspirin (100mg Per Day)
  • Tanatril (5mg Per Day)
  • Olmetec (20mg Per Day)
  • Myslee (10mg Per Day)
  • Artist (2.5mg Per Day)
When using Predonine, the patient experienced the following unwanted symptoms/side effects: Arterial Occlusive DiseaseAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Arterial Occlusive Disease, may become evident only after a product is in use by the general population.
Predonine Side Effect Report#7422098-9
Pancytopenia, Asthenia, Blood Creatine Phosphokinase Increased
This Pancytopenia side effect was reported by a physician from Japan. A 79-year-old female patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Predonine (drug dosage: NA), which was initiated on
Feb 20, 2011. Concurrently used drugs:
  • Niacinamide
  • Pepcid Rpd
  • Baktar
  • Minomycin
.After starting to take Predonine the consumer reported adverse symptoms, such as: Pancytopenia, Asthenia, Blood Creatine Phosphokinase IncreasedThese side effects may potentially be related to Predonine.
Predonine Side Effect Report#7414790-7
Cytomegalovirus Enterocolitis
This is a report of a 6-year-old male patient (weight: NA) from Japan, suffering from the following health symptoms/conditions: henoch-schonlein purpura, who was treated with Predonine (dosage: 2 Mg/kg, Unk, start time: NS), combined with:
  • Methylprednisolone Sodium Succinate (Unk)
and developed a serious reaction and side effect(s): Cytomegalovirus Enterocolitis after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Predonine treatment in male patients, resulting in Cytomegalovirus Enterocolitis side effect. The patient was hospitalized.
Predonine Side Effect Report#7409550-7
Osteomyelitis
This report suggests a potential Predonine Osteomyelitis side effect(s) that can have serious consequences. A 90-year-old female patient (weight: NA) from Japan was diagnosed with the following symptoms/conditions: NA and used Predonine (dosage: NA) starting
Sep 01, 2008. After starting Predonine the patient began experiencing various side effects, including: OsteomyelitisAdditional drugs used concurrently:
  • Alkeran
  • Selbex
  • Zometa
  • Bisphonal
  • Maglax
  • Fosamax
Although Predonine demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Osteomyelitis, may still occur.
Predonine Side Effect Report#7394278-2
Liver Disorder, Dermatitis Acneiform, Infusion Related Reaction
This Liver Disorder problem was reported by a physician from Japan. A 54-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On
Feb 03, 2011 this consumer started treatment with Predonine (dosage: NA). The following drugs were being taken at the same time:
  • Antihistamines (Unk)
When using Predonine, the patient experienced the following unwanted symptoms/side effects: Liver Disorder, Dermatitis Acneiform, Infusion Related ReactionAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Liver Disorder, may become evident only after a product is in use by the general population.
Predonine Side Effect Report#7393750-9
Kidney Transplant Rejection, Infection, Lymphoproliferative Disorder
This Kidney Transplant Rejection side effect was reported by a physician from Japan. A 52-year-old female patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Predonine (drug dosage: NA), which was initiated on
Jul 02, 1998. Concurrently used drugs:
  • Mycophenolate Mofetil (Unk)
  • Prograf
  • Prograf (Unk)
  • Mizoribine
.After starting to take Predonine the consumer reported adverse symptoms, such as: Kidney Transplant Rejection, Infection, Lymphoproliferative DisorderThese side effects may potentially be related to Predonine. The patient was hospitalized.
Predonine Side Effect Report#7386941-4
Dyspnoea, Shock, Asthma
This is a report of a 81-year-old female patient (weight: NA) from Japan, suffering from the following health symptoms/conditions: NA, who was treated with Predonine (dosage: NA, start time:
Mar 07, 2011), combined with:
  • Xyzal (5 Mg Qd Oral)
  • Benet
and developed a serious reaction and side effect(s): Dyspnoea, Shock, Asthma after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Predonine treatment in female patients, resulting in Dyspnoea side effect.
Predonine Side Effect Report#7386373-9
Intraocular Pressure Increased, Osteoporosis, Nephrotic Syndrome, Weight Increased, Hypertension
This report suggests a potential Predonine Intraocular Pressure Increased side effect(s) that can have serious consequences. A 3-year-old male patient (weight: NA) from Japan was diagnosed with the following symptoms/conditions: nephrotic syndrome,hypertension and used Predonine (dosage: 40 Mg,) starting NS. After starting Predonine the patient began experiencing various side effects, including: Intraocular Pressure Increased, Osteoporosis, Nephrotic Syndrome, Weight Increased, HypertensionAdditional drugs used concurrently:
  • Norvasc
  • Neoral (40 Mg,)
  • Steroids Nos (Unk)
Although Predonine demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Intraocular Pressure Increased, may still occur.
Predonine Side Effect Report#7384901-0
Thrombocytopenia, Leukopenia
This Thrombocytopenia problem was reported by a pharmacist from Japan. A 38-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: systemic lupus erythematosus. On
Jul 18, 2010 this consumer started treatment with Predonine (dosage: 30 Mg (daily Dose), , Oral). The following drugs were being taken at the same time: NA. When using Predonine, the patient experienced the following unwanted symptoms/side effects: Thrombocytopenia, LeukopeniaThe patient was hospitalized.Although all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Thrombocytopenia, may become evident only after a product is in use by the general population.
Predonine Side Effect Report#7384833-8
Leukopenia, Thrombocytopenia
This Leukopenia side effect was reported by a physician from Japan. A 38-year-old female patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Predonine (drug dosage: 20 Mg (daily Dose), , Oral), which was initiated on
Jan 01, 2010. Concurrently used drugs:
  • Aspirin (100 Mg (daily Dose), Qd, Oral)
.After starting to take Predonine the consumer reported adverse symptoms, such as: Leukopenia, ThrombocytopeniaThese side effects may potentially be related to Predonine. The patient was hospitalized.
Predonine Side Effect Report#7381607-9
Pneumocystis Jiroveci Pneumonia, Cardiac Failure
This is a report of a male patient (weight: NA) from Japan, suffering from the following health symptoms/conditions: NA, who was treated with Predonine (dosage: NA, start time:
Oct 27, 2010), combined with:
  • Aldactone
  • Metildigoxin
  • Tpn Electrolytes In Plastic Container
  • Dormicum
  • Enteronon-r
  • Artist
  • Furosemide
  • Aspara K
and developed a serious reaction and side effect(s): Pneumocystis Jiroveci Pneumonia, Cardiac Failure after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Predonine treatment in male patients, resulting in Pneumocystis Jiroveci Pneumonia side effect.


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The appearance of Predonine on this list does not mean that FDA has concluded that the drug has the listed risk. It means that FDA has identified a potential safety issue, but it does not mean that FDA has found a causal relationship between the drug and the listed risk.

What are common Predonine Side Effects for Women?

Women Side Effects Reports
Osteomyelitis 6
C-reactive Protein Increased 5
White Blood Cell Count Decreased 5
Herpes Zoster 4
Pancytopenia 4
Ascites 3
Asthma 3
Blood Alkaline Phosphatase Increased 3
Blood Glucose Increased 3
Blood Lactate Dehydrogenase Increased 3

What are common Predonine Side Effects for Men?

Men Side Effects Reports
Blood Creatinine Increased 13
Cerebral Infarction 11
Dysarthria 10
Grip Strength Decreased 10
Jc Virus Infection 9
Leukoaraiosis 9
Progressive Multifocal Leukoencephalopathy 6
Interstitial Lung Disease 5
Renal Impairment 5
Aphasia 4

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Why Your Notes are Important

Your notes could be helpful in several ways:

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  • You will have a record to refer to in the future, in case you are ever prescribed the same medicine again

  • Log Form

    You can use the following log form to write down important information, like the date and time you experienced a side effect and your symptoms, how strong the symptoms were, and any other medicines you were using.

    Medicine Name and Dosage:
    Side Effects Scale Date & Time Other Medicine(s) or Treatment(s)
    Scale: 1 = very mild to 10 = very bad

    Side effects reports are analyzed to discover potential health product safety signals. Some important reactions may take an extremely long time to develop or occur infrequently. Continued monitoring of adverse reactions is thus essential to maintain a comprehensive safety and effectiveness profile of health products.

    You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.

    Predonine reports list potential signals of serious risks and new safety information that were identified using the FDA Adverse Event Reporting System (FAERS).
    FAERS is a database that contains information on adverse event and medication errors reports submitted to FDA by healthcare professionals (such as physicians, pharmacists, nurses and others), consumers (such as patients, family members, layers and others) and manufacturers.

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    Side Effects reported to FDA: 123

    Predonine safety alerts: No

    Reported deaths: 39

    Reported hospitalizations: 64

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