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Dekristol Side Effects

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Common Dekristol Side Effects


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

Bone Pain (5)
Fall (3)
Gait Disturbance (3)
Joint Arthroplasty (2)
Pain (2)
Joint Injury (2)
Dyspnoea (2)
Hospitalisation (2)
Coccydynia (2)
Pelvic Fracture (2)
Peripheral Arterial Occlusive Disease (2)
Surgery (2)
Lumbar Spinal Stenosis (2)
Sensation Of Heaviness (2)
Sciatica (2)
Postoperative Wound Infection (2)
Bacterial Infection (1)
Abdominal Distension (1)
Hypotension (1)
Blood Pressure Increased (1)

➢ 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.

Dekristol Side Effects Reported to FDA



Dekristol Side Effect Report#8448420-2
Breast Cancer
This is a report of a 67-year-old female patient (weight: NA) from Germany, suffering from the following health symptoms/conditions: NA, who was treated with Dekristol (dosage: NA, start time:
May 01, 1997), combined with:
  • Mabthera (4000 Mg)
  • Methotrexate
  • Atacand
and developed a serious reaction and side effect(s): Breast Cancer after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Dekristol treatment in female patients, resulting in Breast Cancer side effect. The patient was hospitalized.
Dekristol Side Effect Report#8369657-7
Pelvic Fracture, Joint Arthroplasty, Postoperative Wound Infection
This report suggests a potential Dekristol Pelvic Fracture side effect(s) that can have serious consequences. A female patient (weight: NA) from Germany was diagnosed with the following symptoms/conditions: osteoporosis,rheumatoid arthritis and used Dekristol (dosage: Qs) starting
Feb 01, 2011. After starting Dekristol the patient began experiencing various side effects, including: Pelvic Fracture, Joint Arthroplasty, Postoperative Wound InfectionAdditional drugs used concurrently:
  • Arcoxia
  • Pantoprazole (40 1x1)
  • Tebesium
  • Cimzia (Number Of Doses Received: 22)
  • Methotrexate Sodium (Qs)
  • Enoxaparin Sodium
  • Prednisolone
  • Methotrexate Sodium (20 Mg/w)
The patient was hospitalized. Although Dekristol demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Pelvic Fracture, may still occur.
Dekristol Side Effect Report#8355006-7
Rheumatoid Arthritis
This Rheumatoid Arthritis problem was reported by a physician from Germany. A 61-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: vitamin d deficiency,rheumatoid arthritis. On
Nov 24, 2011 this consumer started treatment with Dekristol (dosage: 20.000 Ie Weekly). The following drugs were being taken at the same time:
  • Diclofenac
  • Pantoprazole
  • Folsan (5mg Weekly)
  • Folic Acid (5mg Weekly)
  • Pantoprazole
  • Methotrexate
  • Diclofenac
  • Pantoprazole
When using Dekristol, the patient experienced the following unwanted symptoms/side effects: Rheumatoid ArthritisThe 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 Rheumatoid Arthritis, may become evident only after a product is in use by the general population.
Dekristol Side Effect Report#8248448-1
Pulmonary Function Test Decreased, Heart Valve Calcification, Dyspnoea
This Pulmonary Function Test Decreased side effect was reported by a consumer or non-health professional from Germany. A 82-year-old female patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Dekristol (drug dosage: 3 Df, Weekly (1/w)), which was initiated on
Jan 14, 2011. Concurrently used drugs:
  • Antihypertensives
  • Forteo (Unk, Qd)
.After starting to take Dekristol the consumer reported adverse symptoms, such as: Pulmonary Function Test Decreased, Heart Valve Calcification, DyspnoeaThese side effects may potentially be related to Dekristol.
Dekristol Side Effect Report#8239658-8
Joint Arthroplasty, Pelvic Fracture, Postoperative Wound Infection
This is a report of a female patient (weight: NA) from Germany, suffering from the following health symptoms/conditions: osteoporosis,rheumatoid arthritis,antibiotic prophylaxis,thrombosis prophylaxis, who was treated with Dekristol (dosage: Qs, start time:
May 15, 2006), combined with:
  • Arcoxia
  • Tebesium
  • Enoxaparin Sodium
  • Methotrexate Sodium (Qs)
  • Certolizumab Pegol (Number Of Doses Received: 22)
  • Prednisolone
and developed a serious reaction and side effect(s): Joint Arthroplasty, Pelvic Fracture, Postoperative Wound Infection after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Dekristol treatment in female patients, resulting in Joint Arthroplasty side effect. The patient was hospitalized.
Dekristol Side Effect Report#8225827-X
Parathyroidectomy
This report suggests a potential Dekristol Parathyroidectomy side effect(s) that can have serious consequences. A male patient (weight: NA) from Germany was diagnosed with the following symptoms/conditions: NA and used Dekristol (dosage: NA) starting
Oct 27, 2010. After starting Dekristol the patient began experiencing various side effects, including: ParathyroidectomyAdditional drugs used concurrently:
  • Renvela
  • Omeprazole
  • Bisoprolol Fumarate
  • Zemplar
  • Retacrit
  • Simva Basic
  • Fosrenol
  • Ferrelecit
The patient was hospitalized. Although Dekristol demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Parathyroidectomy, may still occur.
Dekristol Side Effect Report#8214634-X
Maternal Exposure During Pregnancy, Ovarian Cyst
This Maternal Exposure During Pregnancy problem was reported by a health professional from Germany. A 0-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On
Aug 03, 2010 this consumer started treatment with Dekristol (dosage: Once Every 14 Days.). The following drugs were being taken at the same time:
  • Levothyroxine Sodium (100 [ug/d ]/ 50ug/d Until March 2011, From March 2011 100ug/d)
  • Metformin Hcl (2000 [mg/d (2x1000) ])
When using Dekristol, the patient experienced the following unwanted symptoms/side effects: Maternal Exposure During Pregnancy, Ovarian CystThe 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 Maternal Exposure During Pregnancy, may become evident only after a product is in use by the general population.
Dekristol Side Effect Report#8181592-6
Fall, Knee Arthroplasty, Vascular Graft, Balance Disorder, Hospitalisation, Asthenia, Blood Pressure Increased
This Fall side effect was reported by a consumer or non-health professional from Germany. A 74-year-old female patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Dekristol (drug dosage: NA), which was initiated on
May 21, 2010. Concurrently used drugs:
  • Humira
  • Ibuprofen Tablets
  • Prednisolone (Unk)
  • Calcium
  • Forteo (Unk, Qd)
.After starting to take Dekristol the consumer reported adverse symptoms, such as: Fall, Knee Arthroplasty, Vascular Graft, Balance Disorder, Hospitalisation, Asthenia, Blood Pressure IncreasedThese side effects may potentially be related to Dekristol. The patient was hospitalized.
Dekristol Side Effect Report#8163104-6
Choking Sensation, Chest Discomfort, Cardiovascular Disorder, Tachycardia, Hypotension, Hypertensive Crisis, Dyspnoea, Hyperhidrosis
This is a report of a male patient (weight: NA) from Germany, suffering from the following health symptoms/conditions: NA, who was treated with Dekristol (dosage: 20000iu Weekly, start time:
Oct 23, 2011), combined with:
  • Votrient (400mg Per Day)
  • Aspirin (100mg Per Day)
  • Amlodipine (5mg Per Day)
  • Diovan (160mg Twice Per Day)
  • Bisoprolol Fumarate (2.5mg Per Day)
  • Simvastatin (20mg Per Day)
and developed a serious reaction and side effect(s): Choking Sensation, Chest Discomfort, Cardiovascular Disorder, Tachycardia, Hypotension, Hypertensive Crisis, Dyspnoea, Hyperhidrosis after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Dekristol treatment in male patients, resulting in Choking Sensation side effect. The patient was hospitalized.
Dekristol Side Effect Report#8133878-9
Sudden Hearing Loss
This report suggests a potential Dekristol Sudden Hearing Loss side effect(s) that can have serious consequences. A 84-year-old female patient (weight: NA) from Germany was diagnosed with the following symptoms/conditions: NA and used Dekristol (dosage: NA) starting
Aug 18, 2010. After starting Dekristol the patient began experiencing various side effects, including: Sudden Hearing LossAdditional drugs used concurrently:
  • Calcium
  • Forteo (Unk, Qd)
The patient was hospitalized. Although Dekristol demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Sudden Hearing Loss, may still occur.
Dekristol Side Effect Report#8113236-3
Hyperkalaemia, Renal Failure Acute, Acidosis
This Hyperkalaemia problem was reported by a consumer or non-health professional from Germany. A 69-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On
Aug 01, 2011 this consumer started treatment with Dekristol (colecalciferol) (dosage: NA). The following drugs were being taken at the same time:
  • Prednisone Tab
  • Adenuric (febuxostat) (120 Milligrams (daily) Oral)
  • Oxycodone Hcl
  • Bondiol (alfacalcidol)
When using Dekristol (colecalciferol), the patient experienced the following unwanted symptoms/side effects: Hyperkalaemia, Renal Failure Acute, AcidosisThe 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 Hyperkalaemia, may become evident only after a product is in use by the general population.
Dekristol Side Effect Report#8019371-2
Spinal Compression Fracture, Bone Pain
This Spinal Compression Fracture side effect was reported by a physician from Germany. A female patient (weight:NA) experienced the following symptoms/conditions: osteoporosis.The patient was prescribed Dekristol (drug dosage: 2000 Iu/week), which was initiated on
Feb 07, 2011. Concurrently used drugs:
  • Zoledronoc Acid (5 Mg Once Yearly)
  • Zoledronoc Acid (5 Mg, Unk)
.After starting to take Dekristol the consumer reported adverse symptoms, such as: Spinal Compression Fracture, Bone PainThese side effects may potentially be related to Dekristol.
Dekristol Side Effect Report#8017348-4
Transplant Rejection
This is a report of a male patient (weight: NA) from Germany, suffering from the following health symptoms/conditions: NA, who was treated with Dekristol (dosage: 1 Dose Form /month, start time:
Dec 10, 2011), combined with:
  • Basiliximab (Last Dose Prior To Sae 17/apr/2011)
  • Metformin Hcl
  • Prednisolone
  • Pantoprazole
  • Bicanorm
  • Tacrolimus (Last Dose Prior To Sae 10/dec/2011)
  • Fluvastatin
  • Repaglinid
and developed a serious reaction and side effect(s): Transplant Rejection after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Dekristol treatment in male patients, resulting in Transplant Rejection side effect. The patient was hospitalized.
Dekristol Side Effect Report#8017069-8
Abdominal Discomfort, Diarrhoea, Syncope, Vasculitis Cerebral, Cerebral Disorder, Abdominal Distension, Regurgitation
This report suggests a potential Dekristol Abdominal Discomfort side effect(s) that can have serious consequences. A male patient (weight: NA) from Germany was diagnosed with the following symptoms/conditions: NA and used Dekristol (dosage: Unk Ukn, Unk) starting
Apr 01, 2011. After starting Dekristol the patient began experiencing various side effects, including: Abdominal Discomfort, Diarrhoea, Syncope, Vasculitis Cerebral, Cerebral Disorder, Abdominal Distension, RegurgitationAdditional drugs used concurrently:
  • Steroids (Unk Ukn, Unk)
  • Myfortic (360 Mg Twice Daily)
  • Angiotensin Ii Antagonists (Unk Ukn, Unk)
The patient was hospitalized. Although Dekristol demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Abdominal Discomfort, may still occur.
Dekristol Side Effect Report#7974412-3
Wrist Fracture, Osteoporotic Fracture, Fall
This Wrist Fracture problem was reported by a physician from Germany. A 85-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On
Feb 15, 2011 this consumer started treatment with Dekristol (dosage: Unk Unk, Qwk). The following drugs were being taken at the same time:
  • Prolia (Unk)
When using Dekristol, the patient experienced the following unwanted symptoms/side effects: Wrist Fracture, Osteoporotic Fracture, FallThe 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 Wrist Fracture, may become evident only after a product is in use by the general population.
Dekristol Side Effect Report#7897134-6
Surgery, Knee Operation, Hospitalisation, Bacterial Infection, Haematoma
This Surgery side effect was reported by a consumer or non-health professional from Germany. A 60-year-old female patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Dekristol (drug dosage: Unk, Weekly (1/w)), which was initiated on
Jan 24, 2011. Concurrently used drugs:
  • Forteo (Unk, Qd)
  • Enbrel
  • Cortisone Acetate (Unk, Prn)
.After starting to take Dekristol the consumer reported adverse symptoms, such as: Surgery, Knee Operation, Hospitalisation, Bacterial Infection, HaematomaThese side effects may potentially be related to Dekristol. The patient was hospitalized.
Dekristol Side Effect Report#7859140-7
C-reactive Protein Increased, Neuroleptic Malignant Syndrome, Blood Creatine Phosphokinase Increased, Pyrexia, Neutropenia, Sepsis, Fall, Gait Disturbance
This is a report of a male patient (weight: NA) from United Kingdom, suffering from the following health symptoms/conditions: vitamin d decreased,schizophrenia, paranoid type,blood cholesterol increased,iron deficiency anaemia,urinary tract disorder,gastrooesophageal reflux disease,salivary hypersecretion,depression, who was treated with Dekristol (dosage: 2 Df, Every 4/52, start time:
Feb 28, 2011), combined with:
  • Clozaril (325 Mg/ Day)
  • Simvastatin (40 Mg/day)
  • Ferrous Sulfate Tab (200 Mg, Tid)
  • Tamsulosin Hydrochloride (400 Ug/ Day)
  • Omeprazole (10 Mg, Bid)
  • Hyoscine Hydrobromide (300 Ug, Tid)
  • Escitalopram (10 Mg/ Day)
and developed a serious reaction and side effect(s): C-reactive Protein Increased, Neuroleptic Malignant Syndrome, Blood Creatine Phosphokinase Increased, Pyrexia, Neutropenia, Sepsis, Fall, Gait Disturbance after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Dekristol treatment in male patients, resulting in C-reactive Protein Increased side effect. The patient was hospitalized.
Dekristol Side Effect Report#7834226-1
Neoplasm Malignant, Neoplasm Progression, Lymphoedema, Lymphangiosis Carcinomatosa, Pain, Renal Failure
This report suggests a potential Dekristol Neoplasm Malignant side effect(s) that can have serious consequences. A male patient (weight: NA) from Germany was diagnosed with the following symptoms/conditions: NA and used Dekristol (dosage: NA) starting
Dec 13, 2010. After starting Dekristol the patient began experiencing various side effects, including: Neoplasm Malignant, Neoplasm Progression, Lymphoedema, Lymphangiosis Carcinomatosa, Pain, Renal FailureAdditional drugs used concurrently:
  • Thyronajod
  • Samarium (2.5 Gbq, Unk)
  • Vinflunine (458 Mg, Unk)
  • Zometa (4 Mg, Every 4 Weeks)
  • Bisoprolol
  • Palladone
  • Gemcitabine Hydrochloride (1830 Mg, Unk)
  • Torsemide (Unk)
Although Dekristol demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Neoplasm Malignant, may still occur.
Dekristol Side Effect Report#7819239-8
Sciatica, Bone Pain, Joint Injury, Lumbar Spinal Stenosis, Peripheral Arterial Occlusive Disease, Coccydynia, Gait Disturbance, Sensation Of Heaviness
This Sciatica problem was reported by a consumer or non-health professional from Germany. A 83-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On
May 12, 2011 this consumer started treatment with Dekristol 20000 (dosage: 1 Unk, Unk). The following drugs were being taken at the same time:
  • Prolia (60 Mg, Unk)
When using Dekristol 20000, the patient experienced the following unwanted symptoms/side effects: Sciatica, Bone Pain, Joint Injury, Lumbar Spinal Stenosis, Peripheral Arterial Occlusive Disease, Coccydynia, Gait Disturbance, Sensation Of HeavinessAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Sciatica, may become evident only after a product is in use by the general population.
Dekristol Side Effect Report#7785629-5
Bone Pain, Lumbar Spinal Stenosis, Peripheral Arterial Occlusive Disease, Gait Disturbance, Sciatica, Joint Injury, Coccydynia, Sensation Of Heaviness
This Bone Pain side effect was reported by a consumer or non-health professional from Germany. A 83-year-old female patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Dekristol 20000 (drug dosage: 1 Unk, Unk), which was initiated on
May 12, 2011. Concurrently used drugs:
  • Prolia (60 Mg, Unk)
.After starting to take Dekristol 20000 the consumer reported adverse symptoms, such as: Bone Pain, Lumbar Spinal Stenosis, Peripheral Arterial Occlusive Disease, Gait Disturbance, Sciatica, Joint Injury, Coccydynia, Sensation Of HeavinessThese side effects may potentially be related to Dekristol 20000.
Dekristol Side Effect Report#7729996-7
Vertebral Wedging, Bone Pain, Thoracic Vertebral Fracture
This is a report of a female patient (weight: NA) from Germany, suffering from the following health symptoms/conditions: osteoporosis, who was treated with Dekristol (dosage: Unk Ukn, Unk, start time:
Dec 15, 2009), combined with:
  • Asthma-spray
  • Zoledronoc Acid (5 Mg, Unk)
and developed a serious reaction and side effect(s): Vertebral Wedging, Bone Pain, Thoracic Vertebral Fracture after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Dekristol treatment in female patients, resulting in Vertebral Wedging side effect.
Dekristol Side Effect Report#7657758-8
Atrial Fibrillation
This report suggests a potential Dekristol Atrial Fibrillation side effect(s) that can have serious consequences. A 64-year-old female patient (weight: NA) from Germany was diagnosed with the following symptoms/conditions: NA and used Dekristol (dosage: 20000 Iu, Weekly) starting
Apr 12, 2010. After starting Dekristol the patient began experiencing various side effects, including: Atrial FibrillationAdditional drugs used concurrently:
  • Prednisolone (7.5 Mg, 1x/day)
  • Methotrexate Sodium (25 Mg, Weekly)
  • Etanercept (50 Mg, Qwk)
The patient was hospitalized. Although Dekristol demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Atrial Fibrillation, may still occur.
Dekristol Side Effect Report#7628596-7
Ureteral Catheterisation, Renal Transplant, Surgery
This Ureteral Catheterisation problem was reported by a physician from Germany. A 67-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On
Mar 17, 2004 this consumer started treatment with Dekristol (dosage: NA). The following drugs were being taken at the same time:
  • Vitamin B6
  • Venofer
  • Simvastatin
When using Dekristol, the patient experienced the following unwanted symptoms/side effects: Ureteral Catheterisation, Renal Transplant, SurgeryThe 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 Ureteral Catheterisation, may become evident only after a product is in use by the general population.
Dekristol Side Effect Report#7611927-1
Bone Infarction
This Bone Infarction side effect was reported by a physician from Germany. A 47-year-old male patient (weight:NA) experienced the following symptoms/conditions: osteoporosis.The patient was prescribed Dekristol (drug dosage: Dose 20000 Ie Freq: Qa), which was initiated on
Mar 01, 2010. Concurrently used drugs:
  • Folic Acid (Route : 144)
  • Alendronic Acid
  • Hydrochlorothiazide-beta
  • Prednisolone
  • Amlodipine
  • Omeprazole (Route 144)
  • Cimzia (No Of Doses Received :21)
  • Methotrexate (Qs)
.After starting to take Dekristol the consumer reported adverse symptoms, such as: Bone InfarctionThese side effects may potentially be related to Dekristol.
Dekristol Side Effect Report#7571013-6
Systemic Lupus Erythematosus
This is a report of a female patient (weight: NA) from Germany, suffering from the following health symptoms/conditions: osteoporosis, who was treated with Dekristol (dosage: NA, start time:
Aug 13, 2009), combined with:
  • Boniva
  • Digitoxin Tab (Frequency 1-0-0)
  • Ramipril (Frequency 1-0-0)
  • Marcumar (According To Inr)
and developed a serious reaction and side effect(s): Systemic Lupus Erythematosus after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Dekristol treatment in female patients, resulting in Systemic Lupus Erythematosus side effect.


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The appearance of Dekristol 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.


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    Medicine Name and Dosage:
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    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.

    Dekristol 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: 29

    Dekristol safety alerts: No

    Reported hospitalizations: 18

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