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Index of reports
> Cases resulting in hospitalization (35)
> Cases with Loss of Consciousness (9)
Below is the selection of adverse event reports related to Esidrix (Hydrochlorothiazide) that includes cases resulting in hospitalization where reactions include loss of consciousness.
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 65 year old female receiving Esidrix (Hydrochlorothiazide)
Reported by a individual with unspecified qualification from France on 2007-05-31
Patient: 65 year old female, weighing 51.0 kg (112.2 pounds)
Adverse reactions / side effects: Nausea, Hyponatraemia, Condition Aggravated, Hypokalaemia, Loss of Consciousness, Renal Impairment, Malaise, Anorexia, Bradycardia, Blood Creatinine Increased, Asthenia
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Esidrix (Hydrochlorothiazide)
Other drugs received by patient: Lasix; Cellcept; Cortancyl; Cardensiel; Triatec; Cozaar; Levothyroxine Sodium; Mediator; Omeprazole; Plavix; Fosamax; Prograf; DI-Antalvic; Noroxin; Insulin
Adverse event in 65 year old female receiving Esidrix (Hydrochlorothiazide)
Reported by a individual with unspecified qualification from France on 2007-05-31
Patient: 65 year old female, weighing 51.0 kg (112.2 pounds)
Adverse reactions / side effects: Nausea, Hyponatraemia, Condition Aggravated, Hypokalaemia, Loss of Consciousness, Renal Impairment, Malaise, Anorexia, Bradycardia, Blood Creatinine Increased, Asthenia
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Esidrix (Hydrochlorothiazide)
Other drugs received by patient: Lasix; Cellcept; Cortancyl; Cardensiel; Triatec; Cozaar; Levothyroxine Sodium; Mediator; Omeprazole; Plavix; Fosamax; Prograf; DI-Antalvic; Noroxin; Insulin
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 65 year old female receiving Esidrix (Hydrochlorothiazide)
Reported by a individual with unspecified qualification from France on 2007-04-20
Patient: 65 year old female, weighing 51.0 kg (112.2 pounds)
Adverse reactions / side effects: Nausea, Hyponatraemia, Hypokalaemia, Loss of Consciousness, Renal Impairment, Malaise, Anorexia, Bradycardia, Asthenia, Blood Creatinine Increased
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Esidrix (Hydrochlorothiazide)
Other drugs received by patient: Lasix; Cellcept; Cortancyl; Cardensiel; Triatec; Cozaar; Levothyroxine Sodium; Mediator; Omeprazole; Plavix; Fosamax; Prograf; DI-Antalvic; Noroxin; Insulin
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 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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