Drugs Associated with Condition Aggravated Side Effect


Although all health products are carefully tested before they are licensed for sale, they can carry various risks. Some side effects may only become evident after a product is in use by the general population.

The following drugs are associated with Condition Aggravated (click on the link below to view detailed reports):

Drug Name Condition Aggravated Reports All Reports
Enbrel 1704 266818
Avonex 1506 158045
Rebif 1007 61131
Tracleer 542 28883
Humira 473 272927
Effexor 436 23726
Pristiq 394 16715
Forteo 383 61427
Abreva 355 4786
Xyrem 347 14347
Byetta 307 119951
Celebrex 282 33182
Lyrica 282 79654
Avandia 268 97096
Lantus 261 26270
Zyprexa 254 36339
Neurontin 252 20785
Tysabri 215 196525
Remicade 208 88892
Suboxone 198 17080
Keppra 191 12843
Velcade 190 27016
Nexium 187 64024
Citalopram 186 21507
Vioxx 184 163906
Betaseron 182 27282
Sertraline 168 13894
Lipitor 165 48673
Cymbalta 162 42505
Zoloft 160 20824
Revlimid 159 67826
Lexapro 157 10929
Mirvaso 156 1233
Fluoxetine 149 11913
Lamotrigine 146 13077
Natalizumab 138 7192
Seroquel 138 83831
Bextra 137 14705
Advair 135 27880
Methotrexate 129 21012
1 of 61  View All


DISCLAIMER: ALL DATA PROVIDED AS-IS, refer to terms of use for additional information.

Condition Aggravated Reports Submitted to FDA

The following Condition Aggravated Side Effect Reports were submitted to FDA by healthcare professionals (physicians, pharmacists, and nurses), consumers (patients, family members, and lawyers) and manufacturers.

This information could help you understand how symptoms, such as Condition Aggravated could occur, develop and what you can do about them.

Condition Aggravated, Bone Neoplasm Malignant

This is a report of a 28-year-old patient (weight: NA) from ISRAEL, suffering from the following symptoms/conditions: psoriatic arthropathy, who was treated with Enbrel (dosage: 50 Mg, Unk, Pre-filled Syringe, start time: Dec 01, 2010), combined with: NA. and developed a serious reaction and side effect(s). The consumer presented with:
  • Condition Aggravated
  • Bone Neoplasm Malignant
which developed after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Enbrel treatment in patients, resulting in Condition Aggravated side effect.
Epilepsy, Condition Aggravated, Diabetes Mellitus

This report suggests a potential Avonex Epilepsy, Condition Aggravated, Diabetes Mellitus side effect(s) that can have serious consequences. A 25-year-old female patient (weight: NA) from UNITED STATES was diagnosed with the following symptoms/conditions: multiple sclerosis and used Avonex (dosage: NA) starting Apr 01, 2011. Soon after starting Avonex the patient began experiencing various side effects, including:
  • Epilepsy
  • Condition Aggravated
  • Diabetes Mellitus
Drugs used concurrently: NA.The patient was hospitalized. Although Avonex demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Condition Aggravated, may still occur.
Condition Aggravated, Poisoning, Multiple Sclerosis, Wheelchair User, Feeling Abnormal, Paraesthesia

This Condition Aggravated, Poisoning, Multiple Sclerosis, Wheelchair User, Feeling Abnormal, Paraesthesia problem was reported by a consumer or non-health professional from UNITED STATES. A female patient (weight: NA) was diagnosed with the following symptoms/conditions: multiple sclerosis. On Mar 20, 2011 this consumer started treatment with Rebif (dosage: 44 Mcg 3 X Week). The following drugs were being taken at the same time: NA. When commencing Rebif, the patient experienced the following unwanted symptoms/side effects:
  • Condition Aggravated
  • Poisoning
  • Multiple Sclerosis
  • Wheelchair User
  • Feeling Abnormal
  • Paraesthesia
Although all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Condition Aggravated, may become evident only after a product is in use by the general population.
Condition Aggravated, Pulmonary Arterial Hypertension

This is a report of a 41-year-old patient (weight: NA) from UNITED STATES. The patient developed the following symptoms/conditions: pulmonary arterial hypertension and was treated with Tracleer (dosage: Oral) starting Jul 27, 2010. Concurrently used drugs:
  • Revatio
Soon after that, the consumer experienced the following side effects:
  • Condition Aggravated
  • Pulmonary Arterial Hypertension
The patient was hospitalized. This opens a possibility that Tracleer treatment could cause the above reactions, including Condition Aggravated, and some subjects may be more susceptible.
Myocardial Infarction, Septic Shock, Confusional State, Pneumonia, Cellulitis, Cardiac Failure Congestive, Condition Aggravated, Hypotension, Oedema Peripheral

A patient (weight: NA) from UNITED STATES with the following symptoms/conditions: psoriatic arthropathy started Humira treatment (dosage: NA) on NS. Soon after starting Humira treatment, the subject experienced various side effects, including:
  • Myocardial Infarction
  • Septic Shock
  • Confusional State
  • Pneumonia
  • Cellulitis
  • Cardiac Failure Congestive
  • Condition Aggravated
  • Hypotension
  • Oedema Peripheral
Concurrently used drugs:
  • Muscle Relaxant
The patient was hospitalized. This finding indicates that some patients could be more vulnerable to Humira.
Fatigue, Condition Aggravated, Off Label Use, Swelling Face, Oropharyngeal Swelling

A patient from UNITED STATES (weight: NA) experienced symptoms, such as: depression,lip swelling and was treated with Effexor Xr(dosage: NA). The treatment was initiated on Apr 01, 2012. After that a consumer reported the following side effect(s):
  • Fatigue
  • Condition Aggravated
  • Off Label Use
  • Swelling Face
  • Oropharyngeal Swelling
Concurrently used drugs, which potentially could have contributed to side effect(s) or affected Effexor Xr efficacy:
  • Benadryl
Arthropathy, Dry Eye, Muscle Tightness, Pain In Extremity, Condition Aggravated, Joint Crepitation, Rash Erythematous, Oropharyngeal Pain

In this report, Pristiq was administered for the following condition: anxiety.A female consumer from UNITED STATES (weight: NA) started Pristiq treatment (dosage: NA) on Oct 20, 2011.Sometime after starting the treatment, the patient complained of the following side effect(s):
  • Arthropathy
  • Dry Eye
  • Muscle Tightness
  • Pain In Extremity
  • Condition Aggravated
  • Joint Crepitation
  • Rash Erythematous
  • Oropharyngeal Pain
A possible interaction with other drugs could have contributed to this reaction:
  • Prednisone Tab
  • Levoxyl
  • Multi-vitamins
  • Humira
  • Flaxseed Oil
Establishing a causal relationship between a specific drug and consumer's side effects is complex, but it is possible that in this report Pristiq treatment could be related to the listed above side effect(s).
Condition Aggravated

This is a report of the following Forteo side effect(s):
  • Condition Aggravated
A 85-year-old patient from FRANCE (weight: NA) presented with the following condition: osteoporosis and received a treatment with Forteo (dosage: 20 Ug, Qd) starting: Apr 21, 2011.The following concurrently used drugs could have generated interactions: NA.This report suggests that a Forteo treatment could be associated with the listed above side effect(s).

This report was submitted by a consumer from (weight: NA). The patient was diagnosed with: NA and was administered (dosage: NA) starting: NS. The consumer developed a set of symptoms:
    Other drugs used simultaneously: NA.Those unexpected symptoms could be linked to a treatment, however establishing a potential drug-safety problem requires a more detailed clinical analysis.
    Colitis Microscopic, Autoimmune Disorder, Condition Aggravated, Limb Injury, Medical Device Complication, Exostosis, Feeling Abnormal, Insomnia, Ligament Rupture

    This is a report of a possible correlation between Xyrem use and the following symptoms/side effect(s):
    • Colitis Microscopic
    • Autoimmune Disorder
    • Condition Aggravated
    • Limb Injury
    • Medical Device Complication
    • Exostosis
    • Feeling Abnormal
    • Insomnia
    • Ligament Rupture
    which could contribute to an assessment of Xyrem risk profile.A 43-year-old female consumer from US (weight: NA) was suffering from narcolepsy and was treated with Xyrem (dosage: 9 Gm (4.5 Gm, 2 In 1 D), Oral) starting Nov 05, 2010.Other concurrent medications: NA.The patient was hospitalized.
    Asthenia, Bipolar Disorder, Condition Aggravated, Dizziness, Injection Site Haematoma, Laceration, Nausea, Overdose, Suicide Attempt

    A female patient from UNITED STATES (weight: NA) presented with the following symptoms: type 2 diabetes mellitus and after a treatment with Byetta (dosage: Unk, Unk) experienced the following side effect(s):
    • Asthenia
    • Bipolar Disorder
    • Condition Aggravated
    • Dizziness
    • Injection Site Haematoma
    • Laceration
    • Nausea
    • Overdose
    • Suicide Attempt
    The treatment was started on May 01, 2006. Byetta was used in combination with the following drugs: NA.The patient was hospitalized.This report could alert potential Byetta consumers.
    Arthralgia, Bacterial Infection, Condition Aggravated, Musculoskeletal Pain, Pruritus, Rash, Rheumatoid Arthritis, Urticaria

    In this report, a female patient from UNITED STATES (weight: NA) was affected by a possible Celebrex side effect.The patient was diagnosed with rheumatoid arthritis. After a treatment with Celebrex (dosage: 200 Mg, 1x/day, start date: Oct 01, 2010), the patient experienced the following side effect(s):
    • Arthralgia
    • Bacterial Infection
    • Condition Aggravated
    • Musculoskeletal Pain
    • Pruritus
    • Rash
    • Rheumatoid Arthritis
    • Urticaria
    The following simultaneously used drugs could have led to this reaction:
    • Oxycodone (30 Mg, Unk)
    The findings here stress that side effects should be taken into consideration when evaluating a Celebrex treatment.
    Visual Acuity Reduced, Vitreous Floaters, Visual Field Defect, Condition Aggravated

    This is a report of a 68-year-old patient from JAPAN (weight: NA), who used Lyrica (dosage: Unk) for a treatment of pain. After starting a treatment on Apr 13, 2012, the patient experienced the following side effect(s):
    • Visual Acuity Reduced
    • Vitreous Floaters
    • Visual Field Defect
    • Condition Aggravated
    The following drugs could possibly have interacted with the Lyrica treatment NA.Taken together, these observations suggest that a Lyrica treatment could be related to side effect(s), such as Visual Acuity Reduced, Vitreous Floaters, Visual Field Defect, Condition Aggravated.
    Cardiac Failure Congestive, Condition Aggravated, Myocardial Infarction, Oedema Peripheral

    This Condition Aggravated side effect was reported by a physician from UNITED STATES. A 60-year-old female patient (weight:NA) experienced the following symptoms/conditions: diabetes mellitus. The patient was prescribed Avandia (dosage: NA), which was started on Apr 01, 2002. Concurrently used drugs: NA. When starting to take Avandia the consumer reported the following symptoms:
    • Cardiac Failure Congestive
    • Condition Aggravated
    • Myocardial Infarction
    • Oedema Peripheral
    The patient was hospitalized. These side effects may potentially be related to Avandia.
    Myocardial Infarction, Diabetic Foot, Condition Aggravated, Depressed Mood

    This is a Lantus side effect report of a 73-year-old patient (weight:NA) from MEXICO, suffering from the following symptoms/conditions: type 2 diabetes mellitus, who was treated with Lantus (dosage:NA, start time: NS), combined with:
    • Glimepiride
    , and developed a serious reaction and a Condition Aggravated side effect. The patient presented with:
    • Myocardial Infarction
    • Diabetic Foot
    • Condition Aggravated
    • Depressed Mood
    which developed after the beginning of treatment. The patient was hospitalized and became disabled. This side effect report can indicate a possible existence of increased vulnerability to Lantus treatment in patients suffering from type 2 diabetes mellitus, resulting in Condition Aggravated.
    Hepatic Failure, Hepatic Enzyme Increased, Jaundice, Condition Aggravated

    This report suggests a potential Zyprexa Condition Aggravated side effect(s) that can have serious consequences. A 52-year-old patient from DENMARK (weight:NA) was diagnosed with the following health condition(s): depression,hypertension,mental disorder and used Zyprexa (dosage: 5 Mg) starting Jan 01, 2012. Soon after starting Zyprexa the patient began experiencing various side effects, including:
    • Hepatic Failure
    • Hepatic Enzyme Increased
    • Jaundice
    • Condition Aggravated
    Drugs used concurrently:
    • Rasilez Hct (150mg/12.5 Mg Daily)
    • Alprazolam (0.75 Mg)
    • Escitalopram (20 Mg)
    • Anafranil (37.5 Mg)
    • Prazepam
    The patient was hospitalized. Although Zyprexa demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Condition Aggravated, may still occur.
    Disability, Obsessive-compulsive Disorder, Compulsive Shopping, Mania, Malaise, Flight Of Ideas, Syncope, Condition Aggravated, Headache

    This Condition Aggravated problem was reported by a health professional from FRANCE. A patient (weight: NA) was diagnosed with the following medical condition(s): epilepsy,restless legs syndrome.On Feb 01, 2010 a consumer started treatment with Neurontin (dosage: NA). The following drugs/medications were being taken at the same time:
    • Ropinirole Hydrochloride (1mg Per Day)
    • Effexor (75mg Per Day)
    When commencing Neurontin, the patient experienced the following unwanted symptoms /side effects:
    • Disability
    • Obsessive-compulsive Disorder
    • Compulsive Shopping
    • Mania
    • Malaise
    • Flight Of Ideas
    • Syncope
    • Condition Aggravated
    • Headache
    The patient was hospitalized. Although all drugs are carefully tested before they are licensed for use, they carry potential side effect risks. Some side effects, such as Condition Aggravated, may become evident only after a product is in use by the general population.
    Condition Aggravated

    This is a Tysabri side effect report of a 37-year-old female patient (weight: NA) from UNITED STATES. The patient developed the following symptoms/conditions: multiple sclerosis and was treated with Tysabri (dosage: NA) starting Mar 02, 2010. Concurrently used drugs: NA. Soon after that, the consumer experienced the following of symptoms:
    • Condition Aggravated
    This opens a possibility that Tysabri could cause Condition Aggravated and that some female patients may be more susceptible.
    Condition Aggravated, Crohn's Disease

    A patient (weight: NA) from CANADA with the following symptoms: crohn's disease started Remicade treatment (dosage: NA) on Sep 19, 2011. Soon after starting Remicade treatment, the consumer experienced several side effects, including:
    • Condition Aggravated
    • Crohn's Disease
    . Concurrently used drugs:
    • Calcium
    • Prednisone Tab
    The patient was hospitalized. This finding indicates that some patients can be more vulnerable to developing Remicade side effects, such as Condition Aggravated.
    Off Label Use, Ocular Neoplasm, Chest Pain, Condition Aggravated

    This Condition Aggravated side effect was reported by a consumer or non-health professional from UNITED STATES. A 48-year-old patient (weight:NA) experienced the following symptoms/conditions: pain.The patient was prescribed Suboxone (dosage: NA), which was started on NS. Concurrently used drugs: NA..When starting to take Suboxone the consumer reported symptoms, such as:
    • Off Label Use
    • Ocular Neoplasm
    • Chest Pain
    • Condition Aggravated
    These side effects may potentially be related to Suboxone.
    Acute Sinusitis, Dementia, Condition Aggravated, Encephalopathy

    This is a report of a 85-year-old patient (weight: NA) from UNITED STATES, suffering from the following symptoms/conditions: convulsion, who was treated with Keppra (dosage: 280mg X 3 Day Qhs Po Recent, start time: NS), combined with:
    • Simvastatin
    • Etodolac
    • Altace
    • Prednisone (Recent)
    • Ultram
    • Donepezil Hcl
    • Uloric
    • Risperdal
    and developed a serious reaction and side effect(s). The consumer presented with:
    • Acute Sinusitis
    • Dementia
    • Condition Aggravated
    • Encephalopathy
    which developed after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Keppra treatment in patients, resulting in Condition Aggravated side effect. The patient was hospitalized.
    Productive Cough, Fatigue, Dizziness, Pain In Jaw, Chest Pain, Malaise, Condition Aggravated, Hypotension, Cardiac Failure Congestive

    This report suggests a potential Velcade Productive Cough, Fatigue, Dizziness, Pain In Jaw, Chest Pain, Malaise, Condition Aggravated, Hypotension, Cardiac Failure Congestive side effect(s) that can have serious consequences. A 74-year-old female patient (weight: NA) from UNITED STATES was diagnosed with the following symptoms/conditions: multiple myeloma and used Velcade (dosage: Iv, 1.3 Mg/m2,sc) starting Jan 09, 2012. Soon after starting Velcade the patient began experiencing various side effects, including:
    • Productive Cough
    • Fatigue
    • Dizziness
    • Pain In Jaw
    • Chest Pain
    • Malaise
    • Condition Aggravated
    • Hypotension
    • Cardiac Failure Congestive
    Drugs used concurrently: NA.The patient was hospitalized. Although Velcade demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Condition Aggravated, may still occur.
    Condition Aggravated, Hiatus Hernia, Dyspepsia

    This Condition Aggravated, Hiatus Hernia, Dyspepsia problem was reported by a consumer or non-health professional from BRAZIL. A 63-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: hiatus hernia,dyspepsia. On Jan 01, 2007 this consumer started treatment with Nexium (dosage: NA). The following drugs were being taken at the same time: NA. When commencing Nexium, the patient experienced the following unwanted symptoms/side effects:
    • Condition Aggravated
    • Hiatus Hernia
    • Dyspepsia
    Although all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Condition Aggravated, may become evident only after a product is in use by the general population.
    Condition Aggravated, Cholestatic Liver Injury

    This is a report of a 63-year-old patient (weight: NA) from SWITZERLAND. The patient developed the following symptoms/conditions: depression and was treated with Citalopram Hydrobromide (dosage: NA) starting Sep 01, 2011. Concurrently used drugs:
    • Primperan (switzerland)
    • Lorazepam
    • Rocephin
    • Acetaminophen
    • Zinacef
    • Oxazepam
    • Nexium
    • Imipenem And Cilastatin Sodium
    Soon after that, the consumer experienced the following side effects:
    • Condition Aggravated
    • Cholestatic Liver Injury
    This opens a possibility that Citalopram Hydrobromide treatment could cause the above reactions, including Condition Aggravated, and some subjects may be more susceptible.
    Anxiety, Cardiovascular Disorder, Condition Aggravated, Myocardial Infarction, Pain

    A 64-year-old patient (weight: NA) from UNITED STATES with the following symptoms/conditions: arthritis started Vioxx treatment (dosage: NA) on Jun 01, 2000. Soon after starting Vioxx treatment, the subject experienced various side effects, including:
    • Anxiety
    • Cardiovascular Disorder
    • Condition Aggravated
    • Myocardial Infarction
    • Pain
    Concurrently used drugs:
    • Triamterene
    This finding indicates that some patients could be more vulnerable to Vioxx.
    Abasia, Condition Aggravated, Diplegia, Hypoaesthesia, Multiple Sclerosis

    A 44-year-old female patient from UNITED STATES (weight: NA) experienced symptoms, such as: multiple sclerosis and was treated with Betaseron(dosage: Total Daily Dose: 8 Miu). The treatment was initiated on Oct 30, 2006. After that a consumer reported the following side effect(s):
    • Abasia
    • Condition Aggravated
    • Diplegia
    • Hypoaesthesia
    • Multiple Sclerosis
    Concurrently used drugs, which potentially could have contributed to side effect(s) or affected Betaseron efficacy: NA.The patient was hospitalized.
    Pancreatitis Chronic, Diarrhoea, Condition Aggravated, Vomiting, Nausea

    In this report, Sertraline Hydrochloride was administered for the following condition: autonomic nervous system imbalance,osteochondrosis.A 43-year-old female consumer from RUSSIAN FEDERATION (weight: NA) started Sertraline Hydrochloride treatment (dosage: 50 Mg, Qd) on Sep 20, 2010.Sometime after starting the treatment, the patient complained of the following side effect(s):
    • Pancreatitis Chronic
    • Diarrhoea
    • Condition Aggravated
    • Vomiting
    • Nausea
    A possible interaction with other drugs could have contributed to this reaction:
    • Meloxicam (Unk)
    Establishing a causal relationship between a specific drug and consumer's side effects is complex, but it is possible that in this report Sertraline Hydrochloride treatment could be related to the listed above side effect(s).
    Dizziness, Circulatory Collapse, Interstitial Lung Disease, Dyspnoea Exertional, Akinesia, Oxygen Saturation Decreased, Multi-organ Failure, Condition Aggravated, Pneumonia Bacterial

    This is a report of the following Lipitor side effect(s):
    • Dizziness
    • Circulatory Collapse
    • Interstitial Lung Disease
    • Dyspnoea Exertional
    • Akinesia
    • Oxygen Saturation Decreased
    • Multi-organ Failure
    • Condition Aggravated
    • Pneumonia Bacterial
    A patient from JAPAN (weight: NA) presented with the following condition: hyperlipidaemia,constipation,epilepsy and received a treatment with Lipitor (dosage: 05 Mg, Unk) starting: Feb 08, 2005.The following concurrently used drugs could have generated interactions:
    • Magnesium Oxide (01 G, Unk)
    • Tegretol (100 Mg, Unk)
    • Gleevec (300 Mg Daily)
    • Lasix (20 Mg, Unk)
    • Gleevec (200 Mg Daily)
    • Selbex (150 Mg, Unk)
    • Epadel S (1200 Mg, Unk)
    The patient was hospitalized.This report suggests that a Lipitor treatment could be associated with the listed above side effect(s).
    Pain, Condition Aggravated, Arthralgia, Hyperhidrosis, Myalgia, Tremor, Somnolence, Impaired Work Ability, Mental Impairment

    This Cymbalta report was submitted by a 45-year-old consumer from UNITED STATES (weight: NA). The patient was diagnosed with: major depression and Cymbalta was administered (dosage: 30mg 4x A Day Po) starting: May 01, 2009. The consumer developed a set of symptoms:
    • Pain
    • Condition Aggravated
    • Arthralgia
    • Hyperhidrosis
    • Myalgia
    • Tremor
    • Somnolence
    • Impaired Work Ability
    • Mental Impairment
    Other drugs used simultaneously: NA.Those unexpected symptoms could be linked to a Cymbalta treatment, however establishing a potential drug-safety problem requires a more detailed clinical analysis.
    Condition Aggravated, Liver Disorder

    This is a report of a possible correlation between Zoloft use and the following symptoms/side effect(s):
    • Condition Aggravated
    • Liver Disorder
    which could contribute to an assessment of Zoloft risk profile.A female consumer from DENMARK (weight: NA) was suffering from depression and was treated with Zoloft (dosage: NA) starting Nov 21, 2011.Other concurrent medications:
    • Lexapro (10 Mg)
    • Risperdal (0.5 Ml)
    • Gasmotin
    • Risperdal (1 Ml)
    • Risperdal (1.5 Ml)
    • Lexapro (10 Mg)
    • Ensure Liquid
    • Magmitt (1980 Mg)
    The patient was hospitalized.
    Cough, Pleural Effusion, Fatigue, Condition Aggravated

    A 74-year-old female patient from UNITED STATES (weight: NA) presented with the following symptoms: waldenstrom's macroglobulinaemia and after a treatment with Revlimid (dosage: 10 Mg 1 Cap Daily X21d Oral) experienced the following side effect(s):
    • Cough
    • Pleural Effusion
    • Fatigue
    • Condition Aggravated
    The treatment was started on Apr 06, 2012. Revlimid was used in combination with the following drugs:
    • Beclomethasone Dipropionate
    • Methylprednisolone
    • Dipropionate
    • Benzonolate
    • Hydroquinone
    • Albuterol
    • Fluticasone Propionate
    • Ibuprofen
    This report could alert potential Revlimid consumers.
    Anxiety, Condition Aggravated, Depression

    In this report, a 31-year-old female patient from UNITED STATES (weight: NA) was affected by a possible Lexapro side effect.The patient was diagnosed with bipolar i disorder. After a treatment with Lexapro (dosage: 20 Mg 1 Dly, start date: NS), the patient experienced the following side effect(s):
    • Anxiety
    • Condition Aggravated
    • Depression
    The following simultaneously used drugs could have led to this reaction: NA.The findings here stress that side effects should be taken into consideration when evaluating a Lexapro treatment.

    This is a report of a patient from (weight: NA), who used (dosage: NA) for a treatment of NA. After starting a treatment on NS, the patient experienced the following side effect(s):
      The following drugs could possibly have interacted with the treatment NA.Taken together, these observations suggest that a treatment could be related to side effect(s), such as .
      Depressive Symptom, Product Substitution Issue, Condition Aggravated

      This Condition Aggravated side effect was reported by a consumer or non-health professional from UNITED STATES. A 61-year-old female patient (weight:NA) experienced the following symptoms/conditions: depression. The patient was prescribed Fluoxetine (dosage: 20.0 Mg), which was started on Mar 01, 2012. Concurrently used drugs: NA. When starting to take Fluoxetine the consumer reported the following symptoms:
      • Depressive Symptom
      • Product Substitution Issue
      • Condition Aggravated
      These side effects may potentially be related to Fluoxetine.
      Insomnia, Mania, Anxiety, Agitation, Depression, Condition Aggravated

      This is a Lamotrigine side effect report of a 47-year-old patient (weight:NA) from UNITED STATES, suffering from the following symptoms/conditions: depression,bipolar disorder, who was treated with Lamotrigine (dosage:100 Mg Once A Day Po, start time: Oct 24, 2011), combined with:
      • Bupropion Hcl (150 Mg Once A Day Po)
      , and developed a serious reaction and a Condition Aggravated side effect. The patient presented with:
      • Insomnia
      • Mania
      • Anxiety
      • Agitation
      • Depression
      • Condition Aggravated
      which developed after the beginning of treatment. This side effect report can indicate a possible existence of increased vulnerability to Lamotrigine treatment in patients suffering from depression,bipolar disorder, resulting in Condition Aggravated.
      Condition Aggravated, Dementia, Disease Progression, Urinary Tract Infection

      This report suggests a potential Natalizumab Condition Aggravated side effect(s) that can have serious consequences. A 66-year-old female patient from UNITED STATES (weight:NA) was diagnosed with the following health condition(s): multiple sclerosis and used Natalizumab (dosage: 300 Mg; Qm; Iv) starting Jul 25, 2007. Soon after starting Natalizumab the patient began experiencing various side effects, including:
      • Condition Aggravated
      • Dementia
      • Disease Progression
      • Urinary Tract Infection
      Drugs used concurrently:NA. The patient was hospitalized. Although Natalizumab demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Condition Aggravated, may still occur.
      Tooth Loss, Insomnia, Condition Aggravated, Diabetes Mellitus, Off Label Use

      This Condition Aggravated problem was reported by a consumer or non-health professional from UNITED STATES. A 62-year-old female patient (weight: NA) was diagnosed with the following medical condition(s): sleep disorder.On NS a consumer started treatment with Seroquel (dosage: NA). The following drugs/medications were being taken at the same time: NA. When commencing Seroquel, the patient experienced the following unwanted symptoms /side effects:
      • Tooth Loss
      • Insomnia
      • Condition Aggravated
      • Diabetes Mellitus
      • Off Label Use
      Although all drugs are carefully tested before they are licensed for use, they carry potential side effect risks. Some side effects, such as Condition Aggravated, may become evident only after a product is in use by the general population.
      Condition Aggravated, Depression, Myocardial Infarction

      This is a Bextra side effect report of a 44-year-old female patient (weight: NA) from UNITED STATES. The patient developed the following symptoms/conditions: arthritis and was treated with Bextra (dosage: 10 Mg (20 Mg, 1 In 1 D)) starting Oct 13, 2004. Concurrently used drugs: NA. Soon after that, the consumer experienced the following of symptoms:
      • Condition Aggravated
      • Depression
      • Myocardial Infarction
      The patient was hospitalized. This opens a possibility that Bextra could cause Condition Aggravated and that some female patients may be more susceptible.
      Product Quality Issue, Underdose, Asthma, Condition Aggravated

      A 91-year-old patient (weight: NA) from UNITED STATES with the following symptoms: dyspnoea started Advair Diskus 100/50 treatment (dosage: NA) on Dec 22, 2009. Soon after starting Advair Diskus 100/50 treatment, the consumer experienced several side effects, including:
      • Product Quality Issue
      • Underdose
      • Asthma
      • Condition Aggravated
      . Concurrently used drugs:
      • Albuterol
      This finding indicates that some patients can be more vulnerable to developing Advair Diskus 100/50 side effects, such as Condition Aggravated.
      Lung Neoplasm, Treatment Noncompliance, Rheumatoid Arthritis, Pleural Effusion, Condition Aggravated

      This Condition Aggravated side effect was reported by a physician from JAPAN. A patient (weight:NA) experienced the following symptoms/conditions: rheumatoid arthritis.The patient was prescribed Methotrexate (dosage: NA), which was started on Nov 28, 2011. Concurrently used drugs:
      • Calblock
      • Famotidine
      .When starting to take Methotrexate the consumer reported symptoms, such as:
      • Lung Neoplasm
      • Treatment Noncompliance
      • Rheumatoid Arthritis
      • Pleural Effusion
      • Condition Aggravated
      These side effects may potentially be related to Methotrexate. The patient was hospitalized.

      Discuss Condition Aggravated Side Effects



      Popular Pages

      More Info