DrugLib.com — Drug Information Portal

Rx drug information, pharmaceutical research, clinical trials, news, and more

Vesicare (Solifenacin) - Reports of Side Effects & Adverse Reactions

 



This is an index of reports of adverse events (side effects, adverse reactions, etc.) related to Vesicare (Solifenacin). Click on the relevant link below to view a selection of reports according to the event's seriousness level and/or the nature of the side effect / adverse reaction. Or scroll down to view a sample of recent reports further on this page.

Our database includes reports from Jan 2007 to Dec 2007. The information is not vetted and should not be cosidered as verified clinical evidence.

All cases (527)
     Drug Ineffective (95)Constipation (56)DRY Mouth (54)more >>

Cases resulting in a serious event (188)
     Urinary Retention (19)Drug Eruption (11)Alanine Aminotransferase Increased (10)more >>

Cases resulting in death (12)
     Respiratory Arrest (4)Vomiting (3)Alanine Aminotransferase Increased (3)more >>

Cases resulting in life threatening events (10)
     Torsade DE Pointes (3)Hepatic Function Abnormal (2)Renal Impairment (2)more >>

Cases resulting in hospitalization (74)
     Urinary Retention (16)Pyrexia (8)Alanine Aminotransferase Increased (6)more >>

Cases resulting in disability (16)
     Purpura (4)Vasculitis (4)Muscular Weakness (3)more >>

Cases resulting in other serious reactions (99)
     Drug Eruption (11)Urinary Retention (7)Blood Lactate Dehydrogenase Increased (6)more >>

Below is a sample of reports where side effects / adverse reactions may be related to Vesicare (Solifenacin). For a complete list and/or a specific selection of reports, please use the links in the index above.

Adverse event in 68 year old female receiving Vesicare (Solifenacin)

Reported by a consumer/non-health professional from United States on 2007-10-30

Patient: 68 year old female

Adverse reactions / side effects: Drug Ineffective, Heart Rate Increased, Condition Aggravated, Cystitis, Heart Rate Irregular, Hypertension

Adverse event resulted in: hospitalization

Suspect drug(s):
Vesicare (Solifenacin)

Other drugs received by patient: Insulin Novolin 70 / 30 (Insulin Human Semisynthetic, Insulin Isophane H; Glucophage; Norvasc; Coreg; Clonidine; Nexium; Zoloft; Topamax; Hydrochlorothiazide; Aspirin; Multi-Vitamin; Adalat; Cozaar



Adverse event in female receiving Vesicare (Solifenacin)

Reported by a physician from Japan on 2007-10-24

Patient: female, weighing 46.5 kg (102.3 pounds)

Adverse reactions / side effects: Sick Sinus Syndrome, Hyperkalaemia

Adverse event resulted in: life threatening event

Suspect drug(s):
Enalapril Maleate
    Administration route: Oral
    Indication: Hypertension
    Start date: 2006-04-26

Micardis
    Administration route: Oral
    Indication: Hypertension
    Start date: 2003-01-14
    End date: 2007-08-19

Spironolactone
    Administration route: Oral
    Indication: Cardiac Failure Chronic
    Start date: 2007-08-01
    End date: 2007-08-19

Vesicare
    Administration route: Oral
    Indication: Hypertonic Bladder
    Start date: 2007-02-21
    End date: 2007-08-19

Other drugs received by patient: Herpamine (Denopamine); Diart; Promac (Polaprezinc); Goodmin; Minzain



Adverse event in 74 year old male receiving Vesicare (Solifenacin)

Reported by a physician from Japan on 2007-10-23

Patient: 74 year old male

Adverse reactions / side effects: Interstitial Lung Disease, Haemoptysis, Condition Aggravated

Adverse event resulted in: hospitalization

Suspect drug(s):
Vesicare (Solifenacin)

Other drugs received by patient: Prednisolone; Baktar (Sulfamethoxazole, Trimethoprim) Tablet; Omeprazole



Adverse event in female receiving Vesicare (Solifenacin)

Reported by a physician from Spain on 2007-10-23

Patient: female

Adverse reactions / side effects: Parkinson's Disease

Adverse event resulted in: hospitalization

Suspect drug(s):
Vesicare (Solifenacin)



Adverse event in 75 year old female receiving Vesicare (Solifenacin)

Reported by a consumer/non-health professional from United States on 2007-10-23

Patient: 75 year old female

Adverse reactions / side effects: Agitation, Dyspnoea, Vaginal Abscess, Musculoskeletal Discomfort, Vaginal Haemorrhage, Palpitations, Vision Blurred, Toothache, Urinary Retention, Hypertension

Adverse event resulted in: hospitalization

Suspect drug(s):
Vesicare (Solifenacin)

Other drugs received by patient: Atenolol; Altace; Glimepiride; Gabapentin; Multivitamins (Ergocalciferol Folic Acid, Nicotinamide, Panthenol, THI



Adverse event in 71 year old male receiving Vesicare (Solifenacin)

Reported by a physician from Japan on 2007-10-23

Patient: 71 year old male, weighing 73.4 kg (161.5 pounds)

Adverse reactions / side effects: Erythema Multiforme

Suspect drug(s):
Vesicare (Solifenacin)

Other drugs received by patient: Bayaspirin Tablets; Amaryl; Amlodipine Besylate; Diovan; Urso 250



Adverse event in 81 year old female receiving Vesicare (Solifenacin)

Reported by a physician from Japan on 2007-10-19

Patient: 81 year old female, weighing 48.0 kg (105.6 pounds)

Adverse reactions / side effects: Torsade DE Pointes

Adverse event resulted in: life threatening event

Suspect drug(s):
Vesicare
    Dosage: 5 mg, uid/qd, oral; oral
    Administration route: Oral
    Start date: 2007-01-01
    End date: 2007-01-01

Vesicare
    Dosage: 5 mg, uid/qd, oral; oral
    Administration route: Oral
    Start date: 2007-02-28
    End date: 2007-03-28

Other drugs received by patient: Spiropent (Clenbuterol Hydrochloride); Amlodipine Besylate; Alfarol (Alfacalcidol); Gasport; Strocain (Oxetacaine); Selbex (Teprenone); Marzulene S (Levoglutamide, Sodium Gualenate); Meilax (Ethyl Loflazepate); Cefazolin; Vancomycin; Targocid



Adverse event in 76 year old female receiving Vesicare (Solifenacin)

Reported by a physician from Japan on 2007-10-19

Patient: 76 year old female, weighing 39.8 kg (87.6 pounds)

Adverse reactions / side effects: Dehydration, Incorrect Dose Administered, Dizziness, Blood Pressure Decreased

Suspect drug(s):
Carvedilol
    Dosage: 2.5 mg, uid/qd, oral
    Administration route: Oral
    Indication: Hypertension
    Start date: 2007-07-26
    End date: 2007-07-31

Vesicare
    Dosage: 2.5 mg, uid/qd, oral
    Administration route: Oral
    Indication: Hypertonic Bladder

Other drugs received by patient: Rhythmy (Rilmazafone); Aspirin; Sigmart (Nicorandil); Lansoprazole; Risedronate Sodium; Amlodipine Besylate; Selbex (Teprenone); Isosorbide Mononitrate



Adverse event in 32 year old female receiving Vesicare (Solifenacin)

Reported by a individual with unspecified qualification from United States on 2007-10-18

Patient: 32 year old female

Adverse reactions / side effects: Drug Exposure During Pregnancy, Blighted Ovum, Abortion Spontaneous, Pregnancy

Suspect drug(s):
Baclofen
    Indication: Muscle Spasms
    End date: 2007-03-01

Celexa
    Indication: Depression
    End date: 2007-03-01

Dynacin
    Indication: Sweat Gland Infection
    End date: 2007-03-01

Provigil
    Indication: Fatigue
    End date: 2007-03-01

Rebif
    Dosage: 44 mcg/3 times wkly/sc
    Indication: Multiple Sclerosis
    Start date: 2006-03-14
    End date: 2007-03-01

Relpax
    Dosage: prn
    Indication: Migraine
    End date: 2007-03-01

Seroquel
    Indication: Insomnia
    End date: 2007-03-01

Vesicare
    Indication: Bladder Disorder
    End date: 2007-03-01



Adverse event in 32 year old female receiving Vesicare (Solifenacin)

Reported by a consumer/non-health professional from United States on 2007-10-15

Patient: 32 year old female

Adverse reactions / side effects: Drug Exposure During Pregnancy, Abortion Spontaneous

Suspect drug(s):
Baclofen
    Indication: Muscle Spasms
    End date: 2007-03-01

Celexa
    Indication: Depression
    End date: 2007-03-01

Minocycline(minocycline Hydrochloride
    Indication: Sweat Gland Infection
    End date: 2007-03-01

Provigil
    Indication: Fatigue
    End date: 2007-03-01

Rebif
    Dosage: 44 other, subcutaneous
    Indication: Multiple Sclerosis
    Start date: 2006-03-14
    End date: 2007-03-01

Relpax
    Indication: Migraine
    End date: 2007-03-01

Seroquel
    Indication: Insomnia
    End date: 2007-03-01

Vesicare
    Indication: Urinary Tract Disorder
    End date: 2007-03-01



Adverse event in 87 year old female receiving Vesicare (Solifenacin)

Reported by a physician from Japan on 2007-10-09

Patient: 87 year old female, weighing 30.5 kg (67.1 pounds)

Adverse reactions / side effects: Cystitis Noninfective, Urinary Bladder Haemorrhage

Suspect drug(s):
Vesicare (Solifenacin)

Other drugs received by patient: Bufferin (Aluminium Glycinate) Tablet; Aspara (Aspartate Potassium) Tablet; Depas (Etizolam) Tablet; Persantin (Dipyridamole) Tablet; Gasmotin (Mosapride Citrate) Tablet; Lendormin (Brotizolam) Tablet; Magnesium Oxide (Magnesium Oxide) Powder



Adverse event in 83 year old male receiving Vesicare (Solifenacin)

Reported by a physician from Japan on 2007-10-09

Patient: 83 year old male

Adverse reactions / side effects: Cardiac Failure

Adverse event resulted in: hospitalization

Suspect drug(s):
Vesicare (Solifenacin)

Other drugs received by patient: Candesartan Cilexetil; Piclonadine (Ticlopidine Hydrochloride); Propafenone HCL; Hibon (Riboflavin Tetrabutyrate); Sigmart (Nicorandil); Diltiazem Hydrochloride; Pursennid (Sennoside A+b); Isosorbide Dinitrate; Urief



Adverse event in 85 year old female receiving Vesicare (Solifenacin)

Reported by a physician from Japan on 2007-10-09

Patient: 85 year old female

Adverse reactions / side effects: Rhabdomyolysis, Conjunctival Hyperaemia, Parkinsonism, Renal Failure Acute

Adverse event resulted in: hospitalization

Suspect drug(s):
Gramilil(tiapride Hydrochloride) Tablet, 25mg
    Dosage: 25 mg, bid, oral
    Administration route: Oral
    Indication: Cerebral Infarction
    Start date: 2007-06-08
    End date: 2007-08-03

Paxil
    Dosage: 10 mg, uid/qd, oral
    Administration route: Oral
    Indication: Depression
    Start date: 2007-06-04
    End date: 2007-06-11

Vesicare
    Dosage: 2.5 mg, oral; 2.5 mg, oral
    Administration route: Oral
    Indication: Hypertonic Bladder
    Start date: 2007-06-04
    End date: 2007-06-01

Vesicare
    Dosage: 2.5 mg, oral; 2.5 mg, oral
    Administration route: Oral
    Indication: Hypertonic Bladder
    Start date: 2007-07-09
    End date: 2007-08-03

Other drugs received by patient: Bufferin (Aluminium Glycinate) Tablet; Epadel (Ethyl Icosapentate) PER Oral NOS; Impromen (Bromperidol) Tablet; Alfarol (Alfacalcidol) Capsule; Gefanil (Gefarnate) Capsule; Pursennid (Sennoside A+b) Tablet; Adofeed (Flurbiprofen) Formulation Unknown; Ibuprofen Granule; Kitazemin (Mequitazine) Fine Granule; Marzulene S (Levoglutamide, Sodium Gualenate) Granule; Flomox (Cefcapene Pivoxil Hydrochloride) Tablet; Selbex (Teprenone) Fine Granule



Adverse event in 83 year old female receiving Vesicare (Solifenacin)

Reported by a physician from Japan on 2007-10-09

Patient: 83 year old female

Adverse reactions / side effects: Atrioventricular Block Complete

Adverse event resulted in: hospitalization, disablity

Suspect drug(s):
Vesicare (Solifenacin)

Other drugs received by patient: Aricept; Rize (Clotiazepam) Tablet



Adverse event in 71 year old male receiving Vesicare (Solifenacin)

Reported by a physician from Japan on 2007-10-09

Patient: 71 year old male, weighing 73.4 kg (161.5 pounds)

Adverse reactions / side effects: Erythema Multiforme

Suspect drug(s):
Vesicare (Solifenacin)

Other drugs received by patient: Bayaspirin Tablet; Amaryl; Amlodin (Amlodipine Besilate) Tablet; Diovan; Urso (Ursodeoxycholic Acid) Tablet



Adverse event in 90 year old female receiving Vesicare (Solifenacin)

Reported by a physician from Japan on 2007-10-09

Patient: 90 year old female, weighing 50.0 kg (110.0 pounds)

Adverse reactions / side effects: Dementia, Parkinsonism

Suspect drug(s):
Aricept
    Dosage: 5 mg, uid/qd, oral; 5 mg/d, oral
    Administration route: Oral
    Indication: Dementia
    Start date: 2004-07-09
    End date: 2007-07-21

Aricept
    Dosage: 5 mg, uid/qd, oral; 5 mg/d, oral
    Administration route: Oral
    Indication: Dementia
    Start date: 2007-08-08

Paxil
    Dosage: 20 mg, bid, oral
    Administration route: Oral
    Indication: Depression
    Start date: 2005-09-07
    End date: 2007-07-21

Vesicare
    Dosage: 5 mg, uid/qd, oral; 10 mg, uid/qd,
    Indication: Hypertonic Bladder
    Start date: 2007-06-20
    End date: 2007-07-03

Vesicare
    Dosage: 5 mg, uid/qd, oral; 10 mg, uid/qd,
    Indication: Hypertonic Bladder
    Start date: 2007-07-04
    End date: 2007-07-21

Other drugs received by patient: Calblock (Azelnidipine) Tablet; Tenormin; Blopress (Candesartan Cilexetil) Tablet



Adverse event in 75 year old female receiving Vesicare (Solifenacin)

Reported by a physician from United States on 2007-10-09

Patient: 75 year old female

Adverse reactions / side effects: Agitation, Dyspnoea, Vaginal Abscess, Musculoskeletal Discomfort, Vaginal Haemorrhage, Palpitations, Vision Blurred, Toothache, Urinary Retention, Hypertension

Adverse event resulted in: hospitalization

Suspect drug(s):
Vesicare (Solifenacin)

Other drugs received by patient: Metformin (Metformin Hydrochloride); Glimepiride; Gabapentin; Multivitamins (Ergocalciferol, Folic Acid, Nicotinamide, Panthenol, TH; Atenolol; Altace



Adverse event in 76 year old female receiving Vesicare (Solifenacin)

Reported by a physician from Japan on 2007-10-03

Patient: 76 year old female, weighing 39.8 kg (87.6 pounds)

Adverse reactions / side effects: Dehydration, Procedural Dizziness, Blood Pressure Decreased

Suspect drug(s):
Artist (Carvedilol) Tablet
    Dosage: 2.5 mg, uid/qd, oral
    Start date: 2007-07-26
    End date: 2007-07-31

Vesicare
    Dosage: 2.5 mg, uid/qd, oral
    Administration route: Oral
    Indication: Hypertonic Bladder

Other drugs received by patient: Rhythmy (Rilmazafone) Tablet; Bayaspirin Tablet; Sigmart (Nicorandil) Tablet; Takepron (Lansoprazole) Tablet; Benet (Risedronate Sodium) Tablet; Amlodipine Besylate; Selbex (Teprenone); Isosorbide Mononitrate



Adverse event in female receiving Vesicare (Solifenacin)

Reported by a consumer/non-health professional from United States on 2007-10-02

Patient: female

Adverse reactions / side effects: Abortion Spontaneous

Suspect drug(s):
Baclofen
    Indication: Muscle Spasms

Celexa
    Indication: Depression

Minocycline HCL
    Indication: Sweat Gland Infection

Provigil
    Indication: Fatigue

Rebif
    Indication: Multiple Sclerosis
    Start date: 2006-03-14
    End date: 2007-03-01

Relpax
    Indication: Migraine

Seroquel
    Indication: Insomnia

Vesicare
    Indication: Bladder Disorder



Adverse event in 75 year old female receiving Vesicare (Solifenacin)

Reported by a physician from Japan on 2007-07-30

Patient: 75 year old female, weighing 59.0 kg (129.8 pounds)

Adverse reactions / side effects: Rectal Ulcer, Anaphylactic Shock, Feeling Abnormal, Treatment Noncompliance

Adverse event resulted in: life threatening event

Suspect drug(s):
Choreitou(herbal Extract Nos) Granule
    Dosage: 2.5 mg, tid, oral
    Administration route: Oral
    Indication: Pollakiuria
    Start date: 2007-06-22
    End date: 2007-06-22

Vesicare
    Dosage: 5 mg, uid/qd, oral
    Administration route: Oral
    Indication: Pollakiuria
    Start date: 2007-06-22
    End date: 2007-06-22



Adverse event in male receiving Vesicare (Solifenacin)

Reported by a health professional (non-physician/pharmacist) from Spain on 2007-07-26

Patient: male

Adverse reactions / side effects: Cognitive Disorder

Suspect drug(s):
Vesicare (Solifenacin)



Adverse event in 84 year old female receiving Vesicare (Solifenacin)

Reported by a physician from Japan on 2007-07-26

Patient: 84 year old female, weighing 71.0 kg (156.2 pounds)

Adverse reactions / side effects: Urinary Retention, Pyrexia, Upper Respiratory Tract Inflammation

Adverse event resulted in: hospitalization

Suspect drug(s):
Vesicare (Solifenacin)

Other drugs received by patient: Gaster D Orodispersable CR Tablet; Lipitor; Amlodipine Besylate; Aspirin; Blopress (Candesartan Cilexetil); Lasix; Alfarol (Alfacalcidol)



Adverse event in 75 year old female receiving Vesicare (Solifenacin)

Reported by a physician from Japan on 2007-07-23

Patient: 75 year old female

Adverse reactions / side effects: Rectal Ulcer, Anaphylactic Shock, Feeling Abnormal

Adverse event resulted in: hospitalization

Suspect drug(s):
Choreitou(herbal Extract Nos) PER Oral NOS
    Dosage: 7.5 mg, /d, oral
    Administration route: Oral
    Indication: Pollakiuria
    Start date: 2007-06-22
    End date: 2007-06-22

Vesicare
    Dosage: 5 mg, /d, oral
    Indication: Pollakiuria
    Start date: 2007-06-22
    End date: 2007-06-22



Adverse event in 70 year old female receiving Vesicare (Solifenacin)

Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-07-23

Patient: 70 year old female

Adverse reactions / side effects: Dizziness, Fall

Suspect drug(s):
Vesicare (Solifenacin)

Other drugs received by patient: Aspirin; Codeine Phosphate and Acetaminophen; Gastrocote (Sodium Bicarbonate, Aluminium Hydroxide Gel, Dried, Magnes; Levothyroxine Sodium; Mirtazapine; Omeprazole; Valsartan



Adverse event in 38 year old female receiving Vesicare (Solifenacin)

Reported by a physician from United Kingdom on 2007-07-20

Patient: 38 year old female, weighing 57.0 kg (125.4 pounds)

Adverse reactions / side effects: Chest Pain, DRY Throat, Paraesthesia

Suspect drug(s):
Vesicare (Solifenacin)

-- advertisement -- The American Red Cross
We comply with
HONcode standard.
Verify here.
Home | About Us | Contact Us | Site usage policy | Privacy policy

All Rights reserved - Copyright DrugLib.com, 2006-2009