Diprospan Side Effects

Diprospan Side Effects Reported to FDA

Diprospan Side Effect Report#9948615
Shock

This is a report of a 40-year-old male patient (weight: NA) from CN, suffering from the following health symptoms/conditions: urticaria, who was treated with Diprospan (dosage: 1 Ml Total Daily, start time:

Feb 24, 2014), combined with: NA. and developed a serious reaction and side effect(s): Shock after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Diprospan treatment in male patients, resulting in Shock side effect. The patient was hospitalized.

Diprospan Side Effect Report#9544105
Cushingoid

This report suggests a potential Diprospan Cushingoid side effect(s) that can have serious consequences. A male patient (weight: NA) from CN was diagnosed with the following symptoms/conditions: haemangioma-thrombocytopenia syndrome and used Diprospan (dosage: 1 Ml (7 Mg) Twice A Week) starting NS. After starting Diprospan the patient began experiencing various side effects, including: CushingoidAdditional drugs used concurrently: NA.The patient was hospitalized. Although Diprospan demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Cushingoid, may still occur.

Diprospan Side Effect Report#9543692
Pneumonia, Varicose Ulceration, Arthralgia, Syncope, Hypertension

This Pneumonia problem was reported by a physician from MX. A 64-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: vascular insufficiency. On

May 05, 2012 this consumer started treatment with Diprospan (dosage: 1 Df, Qd). The following drugs were being taken at the same time: NA. When using Diprospan, the patient experienced the following unwanted symptoms/side effects: Pneumonia, Varicose Ulceration, Arthralgia, Syncope, HypertensionThe 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.

Diprospan Side Effect Report#9543579
Anaphylactic Shock

This Anaphylactic Shock side effect was reported by a physician from CN. A 30-year-old female patient (weight:NA) experienced the following symptoms/conditions: urticaria.The patient was prescribed Diprospan (drug dosage: 5 Mg, Once), which was initiated on

Jul 25, 2009. Concurrently used drugs: NA..After starting to take Diprospan the consumer reported adverse symptoms, such as: Anaphylactic ShockThese side effects may potentially be related to Diprospan. The patient was hospitalized.

Diprospan Side Effect Report#9543423
Pneumonia, Renal Pain, Varicose Ulceration, Arthralgia, Syncope, Hypertension

This is a report of a 64-year-old male patient (weight: NA) from MX, suffering from the following health symptoms/conditions: vascular insufficiency, who was treated with Diprospan (dosage: 1 Df, Unk, start time:

May 05, 2012), combined with: NA. and developed a serious reaction and side effect(s): Pneumonia, Renal Pain, Varicose Ulceration, Arthralgia, Syncope, Hypertension after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Diprospan treatment in male patients, resulting in Pneumonia side effect. The patient was hospitalized.

Diprospan Side Effect Report#9543319
Muscle Contracture

This report suggests a potential Diprospan Muscle Contracture side effect(s) that can have serious consequences. A 1-year-old female patient (weight: NA) from CN was diagnosed with the following symptoms/conditions: urticaria papular and used Diprospan (dosage: 0.5 Ml, Unk) starting

Nov 05, 2010. After starting Diprospan the patient began experiencing various side effects, including: Muscle ContractureAdditional drugs used concurrently: NA.The patient was hospitalized. Although Diprospan demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Muscle Contracture, may still occur.

Diprospan Side Effect Report#9543312
Muscle Contracture

This Muscle Contracture problem was reported by a consumer or non-health professional from CN. A 1-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: dermatitis allergic,herpes zoster,osteoarthritis,eczema. On

Mar 05, 2011 this consumer started treatment with Diprospan (dosage: 0.5 Ml, Once). The following drugs were being taken at the same time: NA. When using Diprospan, the patient experienced the following unwanted symptoms/side effects: Muscle ContractureAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Muscle Contracture, may become evident only after a product is in use by the general population.

Diprospan Side Effect Report#9465550
Pulmonary Embolism

This Pulmonary Embolism side effect was reported by a consumer or non-health professional from TR. A 57-year-old female patient (weight:NA) experienced the following symptoms/conditions: diabetes mellitus.The patient was prescribed Diprospan (drug dosage: 2 Ampoules In Every 3 Months), which was initiated on 201008. Concurrently used drugs: NA..After starting to take Diprospan the consumer reported adverse symptoms, such as: Pulmonary EmbolismThese side effects may potentially be related to Diprospan.

Diprospan Side Effect Report#9398746
Palpitations

This is a report of a female patient (weight: NA) from DK, suffering from the following health symptoms/conditions: seasonal allergy, who was treated with Diprospan (dosage: Strength: 7 Mg/ml, start time: NS), combined with: NA. and developed a serious reaction and side effect(s): Palpitations after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Diprospan treatment in female patients, resulting in Palpitations side effect. The patient was hospitalized.

Diprospan Side Effect Report#9343283
Abdominal Discomfort, Eye Swelling, Nausea

This report suggests a potential Diprospan Abdominal Discomfort side effect(s) that can have serious consequences. A 15-year-old male patient (weight: NA) from CN was diagnosed with the following symptoms/conditions: urticaria papular and used Diprospan (dosage: 1 Ml, Qd) starting

Jan 31, 2012. After starting Diprospan the patient began experiencing various side effects, including: Abdominal Discomfort, Eye Swelling, NauseaAdditional drugs used concurrently: NA. Although Diprospan demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Abdominal Discomfort, may still occur.

Diprospan Side Effect Report#9337296
Visual Impairment, Headache, Sleep Disorder, Anger, Constipation, Eye Pain, Renal Impairment, Arthralgia, Back Pain

This Visual Impairment problem was reported by a consumer or non-health professional from DK. A 48-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: rotator cuff syndrome. On

Aug 09, 2011 this consumer started treatment with Diprospan (dosage: Dosis: 2 Ml D. 9.8.11 Og 2 Ml 6.09.11, Styrke: 7 Mg/ml). The following drugs were being taken at the same time: NA. When using Diprospan, the patient experienced the following unwanted symptoms/side effects: Visual Impairment, Headache, Sleep Disorder, Anger, Constipation, Eye Pain, Renal Impairment, Arthralgia, Back PainAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Visual Impairment, may become evident only after a product is in use by the general population.

Diprospan Side Effect Report#8476305-4
Muscle Contracture

This Muscle Contracture side effect was reported by a consumer or non-health professional from China. A 1-year-old male patient (weight:NA) experienced the following symptoms/conditions: herpes zoster,osteoarthritis,dermatitis contact.The patient was prescribed Diprospan (betamethasone Sodium Phosphate/dipropionate) (betamethasone (drug dosage: 1 Ml;im), which was initiated on

Jan 01, 2011. Concurrently used drugs: NA..After starting to take Diprospan (betamethasone Sodium Phosphate/dipropionate) (betamethasone the consumer reported adverse symptoms, such as: Muscle ContractureThese side effects may potentially be related to Diprospan (betamethasone Sodium Phosphate/dipropionate) (betamethasone.

Diprospan Side Effect Report#7782531-X
Osteopenia

This is a report of a 34-year-old male patient (weight: NA) from Denmark, suffering from the following health symptoms/conditions: NA, who was treated with Diprospan (betamethasone Sodium Phosphate/dipropionat) (betamethasone (dosage: 2 Ml; ;iv, start time:

Dec 16, 2009), combined with:

Prednisolone (5 Mg; ;po)

and developed a serious reaction and side effect(s): Osteopenia after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Diprospan (betamethasone Sodium Phosphate/dipropionat) (betamethasone treatment in male patients, resulting in Osteopenia side effect.

Diprospan Side Effect Report#7655520-3
Ocular Hyperaemia, Ocular Discomfort, Lacrimation Increased, Photalgia, Mydriasis

This report suggests a potential Diprospan (betamethasone Sodium Phosphate/dipropionate) Ocular Hyperaemia side effect(s) that can have serious consequences. A 59-year-old female patient (weight: NA) from Mexico was diagnosed with the following symptoms/conditions: post procedural complication,eye inflammation and used Diprospan (betamethasone Sodium Phosphate/dipropionate) (dosage: NA) starting

Jun 25, 2011. After starting Diprospan (betamethasone Sodium Phosphate/dipropionate) the patient began experiencing various side effects, including: Ocular Hyperaemia, Ocular Discomfort, Lacrimation Increased, Photalgia, MydriasisAdditional drugs used concurrently: NA. Although Diprospan (betamethasone Sodium Phosphate/dipropionate) demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Ocular Hyperaemia, may still occur.

Diprospan Side Effect Report#7563251-3
Retinopathy

This Retinopathy problem was reported by a health professional from Denmark. A 45-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: sports injury. On

Apr 01, 2001 this consumer started treatment with Diprospan (betamethasone Sodium Phosphate/dipropionate) (betamethasone (dosage: 0.6 Ml; Once;). The following drugs were being taken at the same time: NA. When using Diprospan (betamethasone Sodium Phosphate/dipropionate) (betamethasone, the patient experienced the following unwanted symptoms/side effects: RetinopathyAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Retinopathy, may become evident only after a product is in use by the general population.

Diprospan Side Effect Report#7480422-5
Muscle Contracture

This Muscle Contracture side effect was reported by a consumer or non-health professional from China. A 1-year-old patient (weight:NA) experienced the following symptoms/conditions: urticaria.The patient was prescribed Diprospan Sp (betamethasone Sodium Phosphate/dipropionate) (betamethas (drug dosage: ; Im), which was initiated on

Nov 01, 2010. Concurrently used drugs: NA..After starting to take Diprospan Sp (betamethasone Sodium Phosphate/dipropionate) (betamethas the consumer reported adverse symptoms, such as: Muscle ContractureThese side effects may potentially be related to Diprospan Sp (betamethasone Sodium Phosphate/dipropionate) (betamethas. The patient was hospitalized.

Diprospan Side Effect Report#7463068-4
Device Breakage, Emotional Distress, Post Procedural Haemorrhage, Injury

This is a report of a 27-year-old female patient (weight: NA) from United States, suffering from the following health symptoms/conditions: NA, who was treated with Diprospan (dosage: NA, start time:

Feb 16, 2010), combined with: NA. and developed a serious reaction and side effect(s): Device Breakage, Emotional Distress, Post Procedural Haemorrhage, Injury after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Diprospan treatment in female patients, resulting in Device Breakage side effect. The patient was hospitalized.

Diprospan Side Effect Report#7328771-5
Hyperaemia, Oedema

This report suggests a potential Diprospan (bethamethasone Sodium Phosphate/dipropionate) Hyperaemia side effect(s) that can have serious consequences. A 20-year-old female patient (weight: NA) from Russian Federation was diagnosed with the following symptoms/conditions: NA and used Diprospan (bethamethasone Sodium Phosphate/dipropionate) (dosage: Im) starting NS. After starting Diprospan (bethamethasone Sodium Phosphate/dipropionate) the patient began experiencing various side effects, including: Hyperaemia, OedemaAdditional drugs used concurrently: NA. Although Diprospan (bethamethasone Sodium Phosphate/dipropionate) demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Hyperaemia, may still occur.

Diprospan Side Effect Report#7325692-9
Convulsion, Dizziness

This Convulsion problem was reported by a health professional from Russian Federation. A 72-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On NS this consumer started treatment with Diprospan (betamethasone Sodium Phosphate/dipropionate) (betamethasone (dosage: Ia). The following drugs were being taken at the same time:

Lidocain (lidocaine Hydrochloride /00033402/) (;ia)
Concor Cor
Noliprel

When using Diprospan (betamethasone Sodium Phosphate/dipropionate) (betamethasone, the patient experienced the following unwanted symptoms/side effects: Convulsion, DizzinessThe 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 Convulsion, may become evident only after a product is in use by the general population.

Diprospan Side Effect Report#7145313-8
Pneumonia

This Pneumonia side effect was reported by a physician from Ukraine. A 3.-year-old patient (weight:NA) experienced the following symptoms/conditions: tonsillitis.The patient was prescribed Diprospan (betamethasone Sodium Phosphate/dipropionate) (betamethasone (drug dosage: 0.3 Ml), which was initiated on

Jan 01, 2010. Concurrently used drugs: NA..After starting to take Diprospan (betamethasone Sodium Phosphate/dipropionate) (betamethasone the consumer reported adverse symptoms, such as: PneumoniaThese side effects may potentially be related to Diprospan (betamethasone Sodium Phosphate/dipropionate) (betamethasone.

Diprospan Side Effect Report#6967387-7
Anaphylactoid Reaction

This is a report of a 10-year-old male patient (weight: NA) from China, suffering from the following health symptoms/conditions: dermatitis atopic, who was treated with Diprospan (betamethasone Sodium Phosphate/dipropionate) (betamethasone (dosage: 1 Ml;once; Im, start time:

Sep 11, 2009), combined with: NA. and developed a serious reaction and side effect(s): Anaphylactoid Reaction after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Diprospan (betamethasone Sodium Phosphate/dipropionate) (betamethasone treatment in male patients, resulting in Anaphylactoid Reaction side effect.

Diprospan Side Effect Report#6960551-2
Anaphylactoid Reaction, Injection Site Erythema

This report suggests a potential Diprospan (betamethasone Sodium Phosphate / Dipropionate) (betamethaso Anaphylactoid Reaction side effect(s) that can have serious consequences. A 43-year-old male patient (weight: NA) from China was diagnosed with the following symptoms/conditions: keloid scar and used Diprospan (betamethasone Sodium Phosphate / Dipropionate) (betamethaso (dosage: 1 Ml, Once) starting

Jun 02, 2010. After starting Diprospan (betamethasone Sodium Phosphate / Dipropionate) (betamethaso the patient began experiencing various side effects, including: Anaphylactoid Reaction, Injection Site ErythemaAdditional drugs used concurrently: NA. Although Diprospan (betamethasone Sodium Phosphate / Dipropionate) (betamethaso demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Anaphylactoid Reaction, may still occur.

Diprospan Side Effect Report#6960546-9
Anaphylactoid Reaction, Cyanosis, Dizziness

This Anaphylactoid Reaction problem was reported by a health professional from China. A 24-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: keloid scar. On

Jul 08, 2010 this consumer started treatment with Diprospan (betamethasone Sodium Phosphate/dipropionate) (betamethasone (dosage: ; Once). The following drugs were being taken at the same time: NA. When using Diprospan (betamethasone Sodium Phosphate/dipropionate) (betamethasone, the patient experienced the following unwanted symptoms/side effects: Anaphylactoid Reaction, Cyanosis, DizzinessAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Anaphylactoid Reaction, may become evident only after a product is in use by the general population.

Diprospan Side Effect Report#6960528-7
Anaphylactoid Reaction

This Anaphylactoid Reaction side effect was reported by a health professional from China. A 54-year-old female patient (weight:NA) experienced the following symptoms/conditions: dermatitis allergic.The patient was prescribed Diprospan (betamethasone Sodium Phosphate/dipropionate) (betamethasone (drug dosage: 1 Ml; Once; Iv), which was initiated on

Jul 06, 2010. Concurrently used drugs: NA..After starting to take Diprospan (betamethasone Sodium Phosphate/dipropionate) (betamethasone the consumer reported adverse symptoms, such as: Anaphylactoid ReactionThese side effects may potentially be related to Diprospan (betamethasone Sodium Phosphate/dipropionate) (betamethasone.

Diprospan Side Effect Report#6959572-5
Anaphylactoid Reaction

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The appearance of Diprospan 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 Diprospan Side Effects for Women?

Women Side Effects	Reports
Headache	5
Dizziness	4
Syncope	4
Chorioretinopathy	3
Nausea	3
Pain In Extremity	3
Pain In Jaw	3
Tremor	3
Agitation	2
Anaphylactic Shock	2

What are common Diprospan Side Effects for Men?

Men Side Effects	Reports
Anaphylactoid Reaction	6
Arthralgia	4
Dizziness	4
Osteomyelitis	3
Cellulitis	2
Dyslalia	2
Fistula	2
Hypertension	2
Injection Site Erythema	2
Injection Site Reaction	2

Track Your Side Effects

Note Your Observations

It is really important to keep track of your health symptoms, right from the time you start a new medicine. You can do it any way you prefer: in a notebook, in a computer file or using our online tool. You should also note down any other medicines you are taking at the same time, because there could be an interaction between these medicines.

Why Your Notes are Important

Your notes could be helpful in several ways:

You can use them to remind you of details that may alert your health care professional(s) to a problem

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.

Diprospan 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.