Please choose an event type to view the corresponding MedsFacts report:

PRODUCT QUALITY ISSUE ( 25 FDA reports)
NAUSEA ( 21 FDA reports)
DIZZINESS ( 19 FDA reports)
HYPERHIDROSIS ( 17 FDA reports)
MALAISE ( 16 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 16 FDA reports)
ABDOMINAL PAIN ( 15 FDA reports)
DEPRESSION ( 15 FDA reports)
CARDIO-RESPIRATORY ARREST ( 14 FDA reports)
DRUG INEFFECTIVE ( 13 FDA reports)
WEIGHT DECREASED ( 13 FDA reports)
WEIGHT INCREASED ( 12 FDA reports)
HALLUCINATION ( 11 FDA reports)
PAIN ( 11 FDA reports)
SOMNOLENCE ( 11 FDA reports)
VOMITING ( 11 FDA reports)
ADVERSE EVENT ( 10 FDA reports)
FATIGUE ( 10 FDA reports)
FEELING ABNORMAL ( 10 FDA reports)
GASTROINTESTINAL DISORDER ( 10 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 10 FDA reports)
ADVERSE DRUG REACTION ( 9 FDA reports)
WITHDRAWAL SYNDROME ( 9 FDA reports)
CHEILITIS ( 8 FDA reports)
RHABDOMYOLYSIS ( 8 FDA reports)
FALL ( 7 FDA reports)
HEADACHE ( 7 FDA reports)
HOMICIDAL IDEATION ( 7 FDA reports)
PALPITATIONS ( 7 FDA reports)
PYREXIA ( 7 FDA reports)
BODY FAT DISORDER ( 6 FDA reports)
DEATH ( 6 FDA reports)
DRUG DOSE OMISSION ( 6 FDA reports)
DYSPNOEA ( 6 FDA reports)
INCONTINENCE ( 6 FDA reports)
NIGHT SWEATS ( 6 FDA reports)
PNEUMONIA ( 6 FDA reports)
SEROTONIN SYNDROME ( 6 FDA reports)
TREATMENT NONCOMPLIANCE ( 6 FDA reports)
ABASIA ( 5 FDA reports)
CARDIAC ARREST ( 5 FDA reports)
CONFUSIONAL STATE ( 5 FDA reports)
CONVULSION ( 5 FDA reports)
DIARRHOEA ( 5 FDA reports)
EATING DISORDER ( 5 FDA reports)
HYPERTENSION ( 5 FDA reports)
NERVOUS SYSTEM DISORDER ( 5 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 5 FDA reports)
OEDEMA PERIPHERAL ( 5 FDA reports)
UNEVALUABLE EVENT ( 5 FDA reports)
ASTHENIA ( 4 FDA reports)
BLOOD GLUCOSE INCREASED ( 4 FDA reports)
COMPLETED SUICIDE ( 4 FDA reports)
CYSTITIS ( 4 FDA reports)
DECREASED APPETITE ( 4 FDA reports)
DIABETES MELLITUS ( 4 FDA reports)
DRY MOUTH ( 4 FDA reports)
GASTRITIS ( 4 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 4 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 4 FDA reports)
INFECTION ( 4 FDA reports)
LIVER DISORDER ( 4 FDA reports)
MENINGITIS ( 4 FDA reports)
MYOCARDIAL INFARCTION ( 4 FDA reports)
OFF LABEL USE ( 4 FDA reports)
PARTIAL SEIZURES ( 4 FDA reports)
PRURITUS ( 4 FDA reports)
SOPOR ( 4 FDA reports)
SPEECH DISORDER ( 4 FDA reports)
SUICIDE ATTEMPT ( 4 FDA reports)
SWOLLEN TONGUE ( 4 FDA reports)
SYNCOPE ( 4 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 4 FDA reports)
THROMBOSIS ( 4 FDA reports)
URINARY TRACT INFECTION ( 4 FDA reports)
URTICARIA ( 4 FDA reports)
ABDOMINAL DISCOMFORT ( 3 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 3 FDA reports)
AGITATION ( 3 FDA reports)
AMNESIA ( 3 FDA reports)
ANXIETY ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
BALANCE DISORDER ( 3 FDA reports)
BEDRIDDEN ( 3 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 3 FDA reports)
COMA ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
DYSKINESIA ( 3 FDA reports)
EMPHYSEMA ( 3 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 3 FDA reports)
HAEMATOCHEZIA ( 3 FDA reports)
HEART RATE INCREASED ( 3 FDA reports)
HYPERCAPNIA ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 3 FDA reports)
OVERDOSE ( 3 FDA reports)
PNEUMONIA HAEMOPHILUS ( 3 FDA reports)
PRODUCT PACKAGING ISSUE ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
RESPIRATORY ACIDOSIS ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
SCHIZOPHRENIA ( 3 FDA reports)
SCIATICA ( 3 FDA reports)
SPINAL COLUMN STENOSIS ( 3 FDA reports)
TENDON PAIN ( 3 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 2 FDA reports)
ABSCESS INTESTINAL ( 2 FDA reports)
AKATHISIA ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 2 FDA reports)
ANGER ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
BRONCHITIS CHRONIC ( 2 FDA reports)
BURSITIS ( 2 FDA reports)
CARPAL TUNNEL SYNDROME ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CHRONIC SINUSITIS ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
CYST ( 2 FDA reports)
DEMENTIA ( 2 FDA reports)
DRUG ABUSE ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
ERECTILE DYSFUNCTION ( 2 FDA reports)
FEAR ( 2 FDA reports)
FIBROMYALGIA ( 2 FDA reports)
FOOT DEFORMITY ( 2 FDA reports)
FOOT FRACTURE ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
HAEMORRHOIDS ( 2 FDA reports)
HALLUCINATION, AUDITORY ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HOSPITALISATION ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPERSOMNIA ( 2 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
JOINT STIFFNESS ( 2 FDA reports)
LIVER INJURY ( 2 FDA reports)
LOCALISED INFECTION ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
LOSS OF CONTROL OF LEGS ( 2 FDA reports)
MENINGIOMA ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
MOOD ALTERED ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ( 2 FDA reports)
MUSCLE RIGIDITY ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 2 FDA reports)
OVARIAN CANCER RECURRENT ( 2 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PARANOIA ( 2 FDA reports)
PENILE OEDEMA ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
POISONING ( 2 FDA reports)
PSYCHOTIC DISORDER ( 2 FDA reports)
PULMONARY MASS ( 2 FDA reports)
PULMONARY MYCOSIS ( 2 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 2 FDA reports)
RIGHT VENTRICULAR FAILURE ( 2 FDA reports)
SCLERODERMA ( 2 FDA reports)
SENSORY LOSS ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
SUBILEUS ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
SWELLING ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
TARDIVE DYSKINESIA ( 2 FDA reports)
TENDON RUPTURE ( 2 FDA reports)
TENDONITIS ( 2 FDA reports)
THINKING ABNORMAL ( 2 FDA reports)
TIBIA FRACTURE ( 2 FDA reports)
TIC ( 2 FDA reports)
TONGUE DRY ( 2 FDA reports)
TOURETTE'S DISORDER ( 2 FDA reports)
TOXIC SKIN ERUPTION ( 2 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 2 FDA reports)
TREMOR ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APPLICATION SITE BURN ( 1 FDA reports)
APPLICATION SITE PERSPIRATION ( 1 FDA reports)
APPLICATION SITE VESICLES ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BACTERIAL TEST POSITIVE ( 1 FDA reports)
BARRETT'S OESOPHAGUS ( 1 FDA reports)
BITE ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BREAKTHROUGH PAIN ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC AMYLOIDOSIS ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CHEMOTHERAPY ( 1 FDA reports)
CHEYNE-STOKES RESPIRATION ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
COMPULSIONS ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CYSTITIS INTERSTITIAL ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DEPENDENCE ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISABILITY ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DISUSE SYNDROME ( 1 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG-INDUCED LIVER INJURY ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
EAR DISORDER ( 1 FDA reports)
ECHOLALIA ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
ENDOMETRIOSIS ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
FEAR OF DEATH ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FOAMING AT MOUTH ( 1 FDA reports)
FOREIGN BODY ASPIRATION ( 1 FDA reports)
FREEZING PHENOMENON ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAIR TEXTURE ABNORMAL ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HUNGER ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
INADEQUATE ANALGESIA ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
LIGAMENT DISORDER ( 1 FDA reports)
MITRAL VALVE REPAIR ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OROPHARYNGEAL SWELLING ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
OVARIAN FAILURE ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PANIC DISORDER ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
POST VIRAL FATIGUE SYNDROME ( 1 FDA reports)
PRODUCT ADHESION ISSUE ( 1 FDA reports)
PRODUCT PACKAGING QUANTITY ISSUE ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PSYCHIATRIC SYMPTOM ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PURULENCE ( 1 FDA reports)
PYURIA ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RECTAL OBSTRUCTION ( 1 FDA reports)
RECTAL STENOSIS ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RETCHING ( 1 FDA reports)
SCRATCH ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SEXUAL DYSFUNCTION ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SKIN CANCER ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
TEARFULNESS ( 1 FDA reports)
THIRST ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
VEIN DISORDER ( 1 FDA reports)
VITAMIN D DEFICIENCY ( 1 FDA reports)

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