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Index of reports
> All cases (40)
> Cases with Fall (11)
Below is the selection of adverse event reports related to Esidrix (Hydrochlorothiazide) that includes all cases where reactions include fall.
Adverse event in male receiving Esidrix (Hydrochlorothiazide)
Reported by a health professional (non-physician/pharmacist) from France on 2007-10-19
Patient: male
Adverse reactions / side effects: Rhabdomyolysis, Malaise, Renal Failure, Hypotension, Cardioactive Drug Level Increased, Fall
Adverse event resulted in: hospitalization
Suspect drug(s):
Perindopril Erbumine
Dosage: daily dose: 4 milligram(s)
Administration route: Oral
Indication: Ill-Defined Disorder
End date: 2006-03-01
Lasix
Dosage: daily dose: unknown
Administration route: Oral
Indication: Ill-Defined Disorder
End date: 2006-02-28
Lasix
Dosage: daily dose: unknown
Administration route: Oral
Start date: 2006-03-01
Esidrix
Dosage: daily dose: 1 dosage form
Administration route: Oral
Indication: Ill-Defined Disorder
End date: 2006-03-01
Digoxin
Dosage: daily dose: unknown; 0.125 mg x 4/week
Administration route: Oral
Indication: Ill-Defined Disorder
End date: 2006-02-28
Other drugs received by patient: Kardegic
Adverse event in 98 year old male receiving Esidrix (Hydrochlorothiazide)
Reported by a individual with unspecified qualification on 2007-10-17
Patient: 98 year old male
Adverse reactions / side effects: Malaise, Renal Failure, Rhabdomyolysis, Hypotension, Cardioactive Drug Level Increased, Fall
Adverse event resulted in: hospitalization
Suspect drug(s):
Lasilix Retard
Administration route: Oral
End date: 2006-03-01
Esidrix
Administration route: Oral
End date: 2006-03-01
Coversyl / 00790701 /
Administration route: Oral
End date: 2006-03-01
Hemigoxine
Administration route: Oral
End date: 2006-03-01
Other drugs received by patient: Kardegic / 00002703 /
Adverse event in 98 year old male receiving Esidrix (Hydrochlorothiazide)
Reported by a individual with unspecified qualification from France on 2007-10-17
Patient: 98 year old male
Adverse reactions / side effects: Bedridden, Blood Creatine Phosphokinase Increased, Blood Urea Increased, Rhabdomyolysis, Cardioactive Drug Level Above Therapeutic, Hypotension, Fall, Malaise, Renal Failure, Fluid Replacement, Dehydration, Myoglobin Blood Increased, Blood Creatinine Increased, Physical Disability
Adverse event resulted in: hospitalization
Suspect drug(s):
Esidrix
Dosage: 25 mg, qd
Administration route: Oral
End date: 2006-03-01
Lasix
Dosage: 60 mg, qd
Administration route: Oral
End date: 2006-03-01
Perindopril Erbumine
Dosage: 4 mg, qd
Administration route: Oral
End date: 2006-03-01
Digoxin
Dosage: 0.125 mg, qw4
Administration route: Oral
End date: 2006-03-01
Other drugs received by patient: Kardegic
Adverse event in 79 year old female receiving Esidrix (Hydrochlorothiazide)
Reported by a physician from France on 2007-07-09
Patient: 79 year old female
Adverse reactions / side effects: General Physical Condition Abnormal, Lupus-Like Syndrome, Fall, Periorbital Haematoma, Loss of Consciousness, Proteinuria, Depression, Sjogren's Syndrome, Renal Failure Acute, Prurigo, Stevens-Johnson Syndrome, White Blood Cell Count Decreased, Biopsy Salivary Gland Abnormal, Hyponatraemia, Staphylococcal Sepsis, Antinuclear Antibody Positive, Conjunctivitis Infective, Rash Erythematous, Dehydration, Asthenia, Anti-SS-A Antibody Positive, Face Injury
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Desloratadine
Dosage: 5 mg; qd; po
Administration route: Oral
Start date: 2006-06-15
End date: 2006-06-19
Arcalion (NO Pref. Name)
Dosage: po
Administration route: Oral
Start date: 2006-06-01
End date: 2006-06-19
Esidrix
End date: 2006-06-19
Primperan TAB
End date: 2006-06-19
Fluconazole
End date: 2006-06-19
Adverse event in 79 year old female receiving Esidrix (Hydrochlorothiazide)
Reported by a individual with unspecified qualification from France on 2007-05-29
Patient: 79 year old female
Adverse reactions / side effects: Pruritus, Lupus-Like Syndrome, Conjunctivitis, Pyrexia, Hypernatraemia, Fall, Loss of Consciousness, Periorbital Haematoma, C-Reactive Protein Increased, Proteinuria, Blood Uric Acid Increased, Dermatitis Bullous, Injury, Erythema Multiforme, Sjogren's Syndrome, Renal Failure Acute, Stevens-Johnson Syndrome, General Physical Health Deterioration, Staphylococcal Sepsis, Epidermolysis, Antinuclear Antibody Positive, Fluid Replacement, Dehydration, Rash Erythematous, Toxic Skin Eruption, Anti-SS-A Antibody Positive, Inflammation
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Arcalion
Dosage: unk, unk
Administration route: Oral
Indication: Depressive Symptom
Start date: 2006-06-01
End date: 2006-06-19
Primperan INJ
End date: 2006-06-19
Triflucan
End date: 2006-06-19
Desloratadine
Dosage: 1 df, qd
Administration route: Oral
Start date: 2006-06-15
End date: 2006-06-19
Esidrix
Dosage: unk, unk
Administration route: Oral
End date: 2006-06-19
Adverse event in 79 year old female receiving Esidrix (Hydrochlorothiazide)
Reported by a physician from France on 2007-05-04
Patient: 79 year old female
Adverse reactions / side effects: Fall, Loss of Consciousness, Proteinuria, Blood Uric Acid Increased, Eyelid Disorder, Depression, Sjogren's Syndrome, Erythema Multiforme, Haematoma, Renal Failure Acute, Stevens-Johnson Syndrome, White Blood Cell Count Decreased, Toxic Epidermal Necrolysis, Hyponatraemia, Staphylococcal Sepsis, Epidermolysis, Antinuclear Antibody Positive, Conjunctivitis Infective, Sialoadenitis, Dehydration, Asthenia, Anti-SS-A Antibody Positive, Face Injury, Toxic Skin Eruption
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Desloratadine
Dosage: 5 mg; qd; po
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2006-06-15
End date: 2006-06-19
Arcalion (NO Pref. Name)
Dosage: po
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2006-06-01
End date: 2006-06-19
Esidrix
Indication: Drug USE FOR Unknown Indication
End date: 2006-06-19
Primperan TAB
Indication: Drug USE FOR Unknown Indication
End date: 2006-06-19
Fluconazole
Indication: Drug USE FOR Unknown Indication
Adverse event in 79 year old female receiving Esidrix (Hydrochlorothiazide)
Reported by a individual with unspecified qualification from France on 2007-04-11
Patient: 79 year old female
Adverse reactions / side effects: Pruritus, Lupus-Like Syndrome, Sodium Retention, Staphylococcal Sepsis, Fall, Loss of Consciousness, Proteinuria, Rash Erythematous, Dermatitis Bullous, Injury, Sjogren's Syndrome, Toxic Skin Eruption, Renal Failure Acute, Stevens-Johnson Syndrome
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Arcalion
Dosage: unk, unk
Administration route: Oral
Start date: 2006-05-01
Primperan INJ
Triflucan
Desloratadine
Esidrix
Administration route: Oral
Adverse event in 87 year old female receiving Esidrix (Hydrochlorothiazide)
Reported by a health professional (non-physician/pharmacist) from France on 2007-03-14
Patient: 87 year old female, weighing 50.0 kg (110.0 pounds)
Adverse reactions / side effects: Malaise, Vertigo, Fall
Adverse event resulted in: hospitalization
Suspect drug(s):
Amlodipine
Administration route: Oral
Xanax
Administration route: Oral
Lasix
Administration route: Oral
Esidrix
Administration route: Oral
Stablon
Administration route: Oral
Claritin
Administration route: Oral
Vastarel
Dosage: daily dose:70mg-freq:daily
Mopral
Dosage: daily dose:20mg-freq:daily
Kardegic
Dosage: daily dose:75mg-freq:daily
Diffu K
Dosage: text:^6^-freq:daily
Adverse event in 87 year old female receiving Esidrix (Hydrochlorothiazide)
Reported by a individual with unspecified qualification from France on 2007-03-12
Patient: 87 year old female, weighing 50.0 kg (110.0 pounds)
Adverse reactions / side effects: Malaise, Wound, Dizziness, Fall
Adverse event resulted in: hospitalization
Suspect drug(s):
Amlodipine
Dosage: 5 mg, qd
Administration route: Oral
Claritin
Dosage: 10 mg, qd
Administration route: Oral
End date: 2007-01-15
Vastarel
Dosage: 35 mg, bid
Administration route: Oral
End date: 2007-01-06
Esidrix
Dosage: 25 mg, qd
Administration route: Oral
Lasix
Dosage: 20 mg/day
Administration route: Oral
Xanax
Dosage: 0.25 mg/day
Administration route: Oral
End date: 2007-01-17
Stablon
Dosage: 12.5 mg, qd
Administration route: Oral
Other drugs received by patient: Mopral; Kardegic
Adverse event in 79 year old female receiving Esidrix (Hydrochlorothiazide)
Reported by a individual with unspecified qualification from France on 2007-03-09
Patient: 79 year old female
Adverse reactions / side effects: Pruritus, Lupus-Like Syndrome, Fall, Loss of Consciousness, Rash Erythematous, Dermatitis Bullous, Injury, Sjogren's Syndrome, Toxic Skin Eruption, Stevens-Johnson Syndrome
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Arcalion
Dosage: unk, unk
Administration route: Oral
Start date: 2006-05-01
Primperan INJ
Triflucan
Desloratadine
Esidrix
Administration route: Oral
Adverse event in 79 year old female receiving Esidrix (Hydrochlorothiazide)
Reported by a physician from France on 2007-03-05
Patient: 79 year old female
Adverse reactions / side effects: Systemic Lupus Erythematosus, Sjogren's Syndrome, Fall, Face Injury, Loss of Consciousness, Stevens-Johnson Syndrome
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Desloratadine
Dosage: po
Administration route: Oral
Arcalion (NO Pref. Name)
Dosage: po
Administration route: Oral
Esidrix
Primperan TAB
Trifulcan (Fluconazole)
Indication: Drug USE FOR Unknown Indication
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