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

RHABDOMYOLYSIS ( 12 FDA reports)
ATRIAL FIBRILLATION ( 6 FDA reports)
FALL ( 6 FDA reports)
FATIGUE ( 6 FDA reports)
DYSPNOEA ( 5 FDA reports)
FLUSHING ( 5 FDA reports)
PAIN IN EXTREMITY ( 5 FDA reports)
ASTHENIA ( 4 FDA reports)
CONTUSION ( 4 FDA reports)
DEPRESSION ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
MEDICATION ERROR ( 4 FDA reports)
PAIN ( 4 FDA reports)
ABASIA ( 3 FDA reports)
ALOPECIA ( 3 FDA reports)
ANXIETY ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
CATARACT ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
PARALYSIS ( 3 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
RASH ( 3 FDA reports)
SPINAL COMPRESSION FRACTURE ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ANGIOPATHY ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BRUXISM ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DRUG DISPENSING ERROR ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
ECONOMIC PROBLEM ( 2 FDA reports)
ERUCTATION ( 2 FDA reports)
EYE DISORDER ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
FAECES DISCOLOURED ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GENERALISED ERYTHEMA ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 2 FDA reports)
LACERATION ( 2 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
OESOPHAGITIS ( 2 FDA reports)
ORAL PAIN ( 2 FDA reports)
OSTEOPOROSIS ( 2 FDA reports)
PAIN IN JAW ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PRESYNCOPE ( 2 FDA reports)
RIB FRACTURE ( 2 FDA reports)
SKIN IRRITATION ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
TARDIVE DYSKINESIA ( 2 FDA reports)
TYPE 2 DIABETES MELLITUS ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
ABSCESS LIMB ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
AGITATION ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALDOLASE INCREASED ( 1 FDA reports)
ANGER ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
APNOEA ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
BACK DISORDER ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD COUNT ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRADYKINESIA ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BREAST INDURATION ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
BREATH ODOUR ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CAROTID BRUIT ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
COGWHEEL RIGIDITY ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COMPULSIVE LIP BITING ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
COUGH ( 1 FDA reports)
DEFORMITY ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DRUG CLEARANCE DECREASED ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
EAR DISCOMFORT ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EYE INFLAMMATION ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
FEAR OF DEATH ( 1 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
HAEMOGLOBIN URINE PRESENT ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
JAW FRACTURE ( 1 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
KNEE DEFORMITY ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MASKED FACIES ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENISCAL DEGENERATION ( 1 FDA reports)
MENISCUS LESION ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
METABOLIC ALKALOSIS ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MULTIPLE INJURIES ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
OCCIPITAL NEURALGIA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
ORAL DISORDER ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PELVIC DISCOMFORT ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROSTATIC DISORDER ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL PAIN ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RHINITIS ALLERGIC ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
RHONCHI ( 1 FDA reports)
ROTATOR CUFF SYNDROME ( 1 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SCOLIOSIS ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPINAL COLUMN STENOSIS ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
STRESS URINARY INCONTINENCE ( 1 FDA reports)
SYNOVIAL CYST ( 1 FDA reports)
TENDON DISORDER ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
TONGUE BITING ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TREMOR ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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