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

PAIN ( 32 FDA reports)
DEPRESSION ( 23 FDA reports)
NAUSEA ( 23 FDA reports)
ANXIETY ( 22 FDA reports)
DRUG INEFFECTIVE ( 21 FDA reports)
FALL ( 20 FDA reports)
INSOMNIA ( 19 FDA reports)
CONDITION AGGRAVATED ( 17 FDA reports)
ARTHRALGIA ( 16 FDA reports)
OEDEMA PERIPHERAL ( 16 FDA reports)
PAIN IN EXTREMITY ( 16 FDA reports)
AGITATION ( 14 FDA reports)
BACK PAIN ( 14 FDA reports)
DIZZINESS ( 14 FDA reports)
WEIGHT INCREASED ( 14 FDA reports)
ASTHENIA ( 13 FDA reports)
DIARRHOEA ( 12 FDA reports)
DRUG DEPENDENCE ( 12 FDA reports)
SOMNOLENCE ( 12 FDA reports)
TREMOR ( 12 FDA reports)
FATIGUE ( 11 FDA reports)
HEADACHE ( 11 FDA reports)
MALAISE ( 11 FDA reports)
VOMITING ( 11 FDA reports)
CHEST PAIN ( 10 FDA reports)
COMPLETED SUICIDE ( 10 FDA reports)
DRUG INTERACTION ( 10 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 10 FDA reports)
HYPOAESTHESIA ( 10 FDA reports)
LOSS OF CONSCIOUSNESS ( 10 FDA reports)
PNEUMONIA ( 10 FDA reports)
ABDOMINAL PAIN UPPER ( 9 FDA reports)
CONFUSIONAL STATE ( 9 FDA reports)
CONSTIPATION ( 9 FDA reports)
DYSPNOEA ( 9 FDA reports)
PARAESTHESIA ( 9 FDA reports)
PYREXIA ( 9 FDA reports)
RASH ( 9 FDA reports)
WEIGHT DECREASED ( 9 FDA reports)
ERYTHEMA ( 8 FDA reports)
FEELING ABNORMAL ( 8 FDA reports)
GAIT DISTURBANCE ( 8 FDA reports)
GROIN PAIN ( 8 FDA reports)
MYOCARDIAL INFARCTION ( 8 FDA reports)
OVERDOSE ( 8 FDA reports)
PANIC ATTACK ( 8 FDA reports)
PARANOIA ( 8 FDA reports)
ABDOMINAL PAIN ( 7 FDA reports)
CARDIAC ARREST ( 7 FDA reports)
CONVULSION ( 7 FDA reports)
DRUG EFFECT DECREASED ( 7 FDA reports)
DRUG TOLERANCE ( 7 FDA reports)
IRRITABILITY ( 7 FDA reports)
MENTAL DISORDER ( 7 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 7 FDA reports)
NERVOUSNESS ( 7 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 7 FDA reports)
RESPIRATORY FAILURE ( 7 FDA reports)
SLEEP DISORDER ( 7 FDA reports)
TREATMENT NONCOMPLIANCE ( 7 FDA reports)
CARDIOMEGALY ( 6 FDA reports)
CONTUSION ( 6 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 6 FDA reports)
DRUG ABUSER ( 6 FDA reports)
INFUSION RELATED REACTION ( 6 FDA reports)
MULTIPLE DRUG OVERDOSE ( 6 FDA reports)
PRURITUS ( 6 FDA reports)
SHOULDER PAIN ( 6 FDA reports)
THINKING ABNORMAL ( 6 FDA reports)
VIRAL INFECTION ( 6 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
ANGER ( 5 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
BLOOD CREATININE INCREASED ( 5 FDA reports)
BLOOD GLUCOSE INCREASED ( 5 FDA reports)
BLOOD PRESSURE INCREASED ( 5 FDA reports)
BURNING SENSATION ( 5 FDA reports)
CHOLELITHIASIS ( 5 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 5 FDA reports)
COORDINATION ABNORMAL ( 5 FDA reports)
DRUG TOXICITY ( 5 FDA reports)
DYSARTHRIA ( 5 FDA reports)
FORMICATION ( 5 FDA reports)
GLOSSITIS ( 5 FDA reports)
GUN SHOT WOUND ( 5 FDA reports)
HAEMOGLOBIN DECREASED ( 5 FDA reports)
HEART RATE INCREASED ( 5 FDA reports)
HYPOREFLEXIA ( 5 FDA reports)
HYPOTENSION ( 5 FDA reports)
INFLAMMATION ( 5 FDA reports)
MYOCLONUS ( 5 FDA reports)
SUICIDAL IDEATION ( 5 FDA reports)
SUICIDE ATTEMPT ( 5 FDA reports)
THERAPY NON-RESPONDER ( 5 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 5 FDA reports)
WHEEZING ( 5 FDA reports)
ABASIA ( 4 FDA reports)
ABNORMAL BEHAVIOUR ( 4 FDA reports)
ANAEMIA ( 4 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 4 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 4 FDA reports)
BLOOD UREA INCREASED ( 4 FDA reports)
COLD SWEAT ( 4 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 4 FDA reports)
DENTAL CARIES ( 4 FDA reports)
DIFFICULTY IN WALKING ( 4 FDA reports)
DISORIENTATION ( 4 FDA reports)
EMOTIONAL DISORDER ( 4 FDA reports)
EXTRASKELETAL OSSIFICATION ( 4 FDA reports)
HAEMATURIA ( 4 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 4 FDA reports)
INCREASED APPETITE ( 4 FDA reports)
LUNG DISORDER ( 4 FDA reports)
MALNUTRITION ( 4 FDA reports)
MOOD SWINGS ( 4 FDA reports)
MUSCLE SPASMS ( 4 FDA reports)
MYALGIA ( 4 FDA reports)
NEPHROLITHIASIS ( 4 FDA reports)
PANCYTOPENIA ( 4 FDA reports)
PHOTOPHOBIA ( 4 FDA reports)
PLEURAL EFFUSION ( 4 FDA reports)
POLLAKIURIA ( 4 FDA reports)
POLYSUBSTANCE ABUSE ( 4 FDA reports)
PRODUCTIVE COUGH ( 4 FDA reports)
PULMONARY CONGESTION ( 4 FDA reports)
PULMONARY OEDEMA ( 4 FDA reports)
SCAB ( 4 FDA reports)
SKIN LESION ( 4 FDA reports)
SKIN ULCER ( 4 FDA reports)
SWELLING ( 4 FDA reports)
TEARFULNESS ( 4 FDA reports)
URINARY TRACT INFECTION ( 4 FDA reports)
ADJUSTMENT DISORDER ( 3 FDA reports)
AFFECT LABILITY ( 3 FDA reports)
AFFECTIVE DISORDER ( 3 FDA reports)
AGGRESSION ( 3 FDA reports)
AMNESIA ( 3 FDA reports)
ANOREXIA ( 3 FDA reports)
ATRIAL FLUTTER ( 3 FDA reports)
BIPOLAR DISORDER ( 3 FDA reports)
BLADDER DISORDER ( 3 FDA reports)
BLOOD POTASSIUM DECREASED ( 3 FDA reports)
BRADYCARDIA ( 3 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 3 FDA reports)
CEREBRAL ISCHAEMIA ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
CONJUNCTIVAL IRRITATION ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
DIABETES MELLITUS ( 3 FDA reports)
DYSPEPSIA ( 3 FDA reports)
EXCORIATION ( 3 FDA reports)
EYE IRRITATION ( 3 FDA reports)
EYE PAIN ( 3 FDA reports)
FEBRILE NEUTROPENIA ( 3 FDA reports)
FIBROMYALGIA ( 3 FDA reports)
FOAMING AT MOUTH ( 3 FDA reports)
GANGLION ( 3 FDA reports)
GASTROENTERITIS ( 3 FDA reports)
HALLUCINATION ( 3 FDA reports)
HELICOBACTER INFECTION ( 3 FDA reports)
HEPATIC STEATOSIS ( 3 FDA reports)
HEPATITIS ( 3 FDA reports)
HERPES ZOSTER ( 3 FDA reports)
HIP FRACTURE ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
HYPOALBUMINAEMIA ( 3 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 3 FDA reports)
INFECTION ( 3 FDA reports)
INFLUENZA ( 3 FDA reports)
INJECTION SITE BRUISING ( 3 FDA reports)
INJURY ( 3 FDA reports)
LETHARGY ( 3 FDA reports)
LUMBAR RADICULOPATHY ( 3 FDA reports)
MAJOR DEPRESSION ( 3 FDA reports)
MEDICATION ERROR ( 3 FDA reports)
MEMORY IMPAIRMENT ( 3 FDA reports)
MENTAL STATUS CHANGES ( 3 FDA reports)
MICTURITION URGENCY ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 3 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 3 FDA reports)
NERVOUS SYSTEM DISORDER ( 3 FDA reports)
NICOTINE DEPENDENCE ( 3 FDA reports)
OESOPHAGITIS ( 3 FDA reports)
ONYCHOLYSIS ( 3 FDA reports)
OSTEOARTHRITIS ( 3 FDA reports)
OVARIAN CYST ( 3 FDA reports)
PELVIC PAIN ( 3 FDA reports)
PENIS DISORDER ( 3 FDA reports)
PERONEAL NERVE PALSY ( 3 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 3 FDA reports)
POLYNEUROPATHY ( 3 FDA reports)
RADIUS FRACTURE ( 3 FDA reports)
RESPIRATORY ARREST ( 3 FDA reports)
RESPIRATORY DISTRESS ( 3 FDA reports)
RESPIRATORY RATE DECREASED ( 3 FDA reports)
RESTLESSNESS ( 3 FDA reports)
SEDATION ( 3 FDA reports)
SOFT TISSUE DISORDER ( 3 FDA reports)
STATUS ASTHMATICUS ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
TINNITUS ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
ABNORMAL DREAMS ( 2 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ADVERSE EVENT ( 2 FDA reports)
AORTIC VALVE INCOMPETENCE ( 2 FDA reports)
APHASIA ( 2 FDA reports)
AREFLEXIA ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
BRAIN OEDEMA ( 2 FDA reports)
BRONCHIAL INFECTION ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
BRONCHITIS CHRONIC ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CEREBRAL ATROPHY ( 2 FDA reports)
CHILLS ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
COMA ( 2 FDA reports)
COUGH ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
DERMATITIS ( 2 FDA reports)
DIABETIC COMPLICATION ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DRUG INTOLERANCE ( 2 FDA reports)
DRUG SCREEN POSITIVE ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 2 FDA reports)
EMOTIONAL DISTRESS ( 2 FDA reports)
FEAR ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
GOITRE ( 2 FDA reports)
GOUT ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HALLUCINATION, VISUAL ( 2 FDA reports)
HEAD INJURY ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HEPATITIS A ( 2 FDA reports)
HEPATITIS B ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
HOSTILITY ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
HYPOMAGNESAEMIA ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
INADEQUATE ANALGESIA ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INJECTION SITE DESQUAMATION ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
INJECTION SITE RASH ( 2 FDA reports)
INTENTIONAL SELF-INJURY ( 2 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 2 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
LEG AMPUTATION ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LISTLESS ( 2 FDA reports)
LOCALISED INFECTION ( 2 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
MELAENA ( 2 FDA reports)
MIGRAINE ( 2 FDA reports)
MULTIPLE SCLEROSIS ( 2 FDA reports)
MYOCARDIAL FIBROSIS ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
OBESITY ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OVARIAN ABSCESS ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 2 FDA reports)
PCO2 INCREASED ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
POISONING DELIBERATE ( 2 FDA reports)
PULMONARY HYPERTENSION ( 2 FDA reports)
RADICULAR PAIN ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
RETINAL DETACHMENT ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
RHINORRHOEA ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
SINUS BRADYCARDIA ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
SPINAL FUSION SURGERY ( 2 FDA reports)
TOOTH EXTRACTION ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
UNRESPONSIVE TO STIMULI ( 2 FDA reports)
UPPER EXTREMITY MASS ( 2 FDA reports)
URINE OUTPUT DECREASED ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
VICTIM OF CHILD ABUSE ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
WHEELCHAIR USER ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 1 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL INJURY ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACUTE ABDOMEN ( 1 FDA reports)
ACUTE SINUSITIS ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ALCOHOLISM ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANAL CANCER ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANXIETY DISORDER ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
ARTERIAL DISORDER ( 1 FDA reports)
ARTHROPOD BITE ( 1 FDA reports)
ASEPTIC NECROSIS BONE ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 1 FDA reports)
ATROPHY ( 1 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BILIARY DILATATION ( 1 FDA reports)
BILIARY SEPSIS ( 1 FDA reports)
BLADDER DISCOMFORT ( 1 FDA reports)
BLADDER OPERATION ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD INSULIN ABNORMAL ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD TEST ABNORMAL ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRADYARRHYTHMIA ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BRAIN STEM INFARCTION ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BRONCHIOLITIS ( 1 FDA reports)
BRONCHITIS ACUTE ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CALCULUS BLADDER ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOTOXICITY ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CATHETER BACTERAEMIA ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CEREBELLAR ATROPHY ( 1 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CHRONIC RESPIRATORY DISEASE ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
COLLAPSE OF LUNG ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CRYING ( 1 FDA reports)
CSF PROTEIN INCREASED ( 1 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CYSTITIS INTERSTITIAL ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEATH OF FRIEND ( 1 FDA reports)
DEATH OF RELATIVE ( 1 FDA reports)
DEMYELINATION ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DEVICE CONNECTION ISSUE ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 1 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DROP ATTACKS ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INTERACTION POTENTIATION ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPHORIA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ENCEPHALITIS ( 1 FDA reports)
ENDOMETRIOSIS ( 1 FDA reports)
ENZYME ABNORMALITY ( 1 FDA reports)
EOSINOPHIL COUNT DECREASED ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
EXERCISE TEST ABNORMAL ( 1 FDA reports)
EXERCISE TOLERANCE DECREASED ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FEEDING DISORDER ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FEMORAL NECK FRACTURE ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 1 FDA reports)
FOOD POISONING ( 1 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
FRUSTRATION ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTRIC OPERATION ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTRIC VARICES ( 1 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 1 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
GENITAL LESION ( 1 FDA reports)
GINGIVAL PAIN ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMATOMA INFECTION ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HANGOVER ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HILAR LYMPHADENOPATHY ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HOMICIDAL IDEATION ( 1 FDA reports)
HUMERUS FRACTURE ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
ILEUS ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
IMPULSIVE BEHAVIOUR ( 1 FDA reports)
INAPPROPRIATE AFFECT ( 1 FDA reports)
INCISION SITE COMPLICATION ( 1 FDA reports)
INCISION SITE HAEMORRHAGE ( 1 FDA reports)
INCISION SITE INFECTION ( 1 FDA reports)
INCISIONAL HERNIA REPAIR ( 1 FDA reports)
INFLUENZA VIRUS TEST POSITIVE ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
ISCHAEMIC HEPATITIS ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
KLEBSIELLA BACTERAEMIA ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
LIGAMENT RUPTURE ( 1 FDA reports)
LIPOMA ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOCKED-IN SYNDROME ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LUNG CANCER METASTATIC ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LYME DISEASE ( 1 FDA reports)
LYMPHANGIOMA ( 1 FDA reports)
MANIA ( 1 FDA reports)
MASS ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
MENINGITIS ASEPTIC ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METABOLIC ALKALOSIS ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
MICROANGIOPATHY ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MINERAL DEFICIENCY ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MITOCHONDRIAL MYOPATHY ACQUIRED ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MOANING ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MONOCYTE COUNT DECREASED ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCLE FATIGUE ( 1 FDA reports)
MUSCLE INJURY ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
NEGATIVISM ( 1 FDA reports)
NEUROMYOPATHY ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
NODULE ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
OSTEOARTHROPATHY ( 1 FDA reports)
OSTEOCHONDROMA ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
OSTEOSARCOMA METASTATIC ( 1 FDA reports)
PARAPLEGIA ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PARTNER STRESS ( 1 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PLEUROPERICARDITIS ( 1 FDA reports)
PNEUMATOSIS INTESTINALIS ( 1 FDA reports)
PNEUMATURIA ( 1 FDA reports)
PNEUMOCEPHALUS ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
PO2 INCREASED ( 1 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 1 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
POSTOPERATIVE INFECTION ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PRESSURE OF SPEECH ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY TOXICITY ( 1 FDA reports)
RAYNAUD'S PHENOMENON ( 1 FDA reports)
RECTAL CANCER ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RENAL ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL HAEMATOMA ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 1 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 1 FDA reports)
SCAN ABNORMAL ( 1 FDA reports)
SCAR ( 1 FDA reports)
SCRATCH ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SELF-INJURIOUS IDEATION ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SINOATRIAL BLOCK ( 1 FDA reports)
SINUS ARRHYTHMIA ( 1 FDA reports)
SINUS HEADACHE ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SKIN PAPILLOMA ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SKULL FRACTURED BASE ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 1 FDA reports)
SLEEP WALKING ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SOCIAL PROBLEM ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPINAL COLUMN STENOSIS ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
SPINAL CORD DISORDER ( 1 FDA reports)
SPUTUM DISCOLOURED ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
STRESS ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUBCUTANEOUS ABSCESS ( 1 FDA reports)
SUBDURAL HAEMORRHAGE ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
THIRST ( 1 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 1 FDA reports)
TOE AMPUTATION ( 1 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 1 FDA reports)
TRANCE ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
TULARAEMIA ( 1 FDA reports)
TUMOUR LYSIS SYNDROME ( 1 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY TRACT DISORDER ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
UTERINE PROLAPSE ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VEIN DISORDER ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 1 FDA reports)
WOUND ( 1 FDA reports)
WOUND HAEMORRHAGE ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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