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

NAUSEA ( 47 FDA reports)
PAIN ( 47 FDA reports)
DYSPNOEA ( 40 FDA reports)
VOMITING ( 40 FDA reports)
MIGRAINE ( 39 FDA reports)
PNEUMONIA ( 36 FDA reports)
CHEST PAIN ( 34 FDA reports)
PULMONARY EMBOLISM ( 34 FDA reports)
ANXIETY ( 32 FDA reports)
HEADACHE ( 31 FDA reports)
DIZZINESS ( 30 FDA reports)
DRUG INEFFECTIVE ( 30 FDA reports)
FATIGUE ( 28 FDA reports)
DEEP VEIN THROMBOSIS ( 27 FDA reports)
INSOMNIA ( 23 FDA reports)
PARAESTHESIA ( 23 FDA reports)
ARTHRALGIA ( 21 FDA reports)
ASTHENIA ( 21 FDA reports)
DEPRESSION ( 21 FDA reports)
HYPOTENSION ( 21 FDA reports)
TREMOR ( 21 FDA reports)
DIARRHOEA ( 20 FDA reports)
INJURY ( 20 FDA reports)
PALPITATIONS ( 19 FDA reports)
EMOTIONAL DISTRESS ( 18 FDA reports)
FEELING ABNORMAL ( 18 FDA reports)
CEREBROVASCULAR ACCIDENT ( 17 FDA reports)
CONFUSIONAL STATE ( 17 FDA reports)
CONSTIPATION ( 17 FDA reports)
FALL ( 17 FDA reports)
HYPOAESTHESIA ( 17 FDA reports)
MALAISE ( 17 FDA reports)
OEDEMA PERIPHERAL ( 16 FDA reports)
URINARY TRACT INFECTION ( 16 FDA reports)
VISION BLURRED ( 16 FDA reports)
WEIGHT INCREASED ( 16 FDA reports)
CHEST DISCOMFORT ( 15 FDA reports)
BALANCE DISORDER ( 14 FDA reports)
PAIN IN EXTREMITY ( 14 FDA reports)
ABNORMAL DREAMS ( 13 FDA reports)
AMNESIA ( 13 FDA reports)
DYSGEUSIA ( 13 FDA reports)
HEART RATE INCREASED ( 13 FDA reports)
LOSS OF CONSCIOUSNESS ( 13 FDA reports)
SINUS BRADYCARDIA ( 13 FDA reports)
WEIGHT DECREASED ( 13 FDA reports)
CHOLELITHIASIS ( 12 FDA reports)
CONVULSION ( 12 FDA reports)
DEHYDRATION ( 12 FDA reports)
DISTURBANCE IN ATTENTION ( 12 FDA reports)
FEMUR FRACTURE ( 12 FDA reports)
HYPERHIDROSIS ( 12 FDA reports)
RASH ( 12 FDA reports)
BACK PAIN ( 11 FDA reports)
IRRITABILITY ( 11 FDA reports)
STAPHYLOCOCCAL INFECTION ( 11 FDA reports)
ABDOMINAL PAIN UPPER ( 10 FDA reports)
ANAEMIA ( 10 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 10 FDA reports)
SOMNOLENCE ( 10 FDA reports)
SYNCOPE ( 10 FDA reports)
UROSEPSIS ( 10 FDA reports)
ABDOMINAL DISCOMFORT ( 9 FDA reports)
DIABETES MELLITUS ( 9 FDA reports)
DRUG EFFECT DECREASED ( 9 FDA reports)
VERTIGO ( 9 FDA reports)
ABDOMINAL DISTENSION ( 8 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 8 FDA reports)
CHOLECYSTITIS ACUTE ( 8 FDA reports)
CHOLECYSTITIS CHRONIC ( 8 FDA reports)
EJECTION FRACTION DECREASED ( 8 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 8 FDA reports)
FEELING COLD ( 8 FDA reports)
HYPERLIPIDAEMIA ( 8 FDA reports)
INFECTION ( 8 FDA reports)
LEUKOCYTOSIS ( 8 FDA reports)
LOW TURNOVER OSTEOPATHY ( 8 FDA reports)
MIGRAINE WITHOUT AURA ( 8 FDA reports)
PHONOPHOBIA ( 8 FDA reports)
PHOTOPHOBIA ( 8 FDA reports)
SINUS ARRHYTHMIA ( 8 FDA reports)
SUICIDAL IDEATION ( 8 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 8 FDA reports)
ABDOMINAL PAIN ( 7 FDA reports)
ALOPECIA ( 7 FDA reports)
BRADYCARDIA ( 7 FDA reports)
CONTUSION ( 7 FDA reports)
DRUG HYPERSENSITIVITY ( 7 FDA reports)
HYPERTENSION ( 7 FDA reports)
MYOCARDIAL INFARCTION ( 7 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 7 FDA reports)
POLYCYSTIC OVARIES ( 7 FDA reports)
PRURITUS ( 7 FDA reports)
BONE DISORDER ( 6 FDA reports)
COUGH ( 6 FDA reports)
DEATH ( 6 FDA reports)
FEELING HOT ( 6 FDA reports)
FRACTURE DISPLACEMENT ( 6 FDA reports)
FRACTURE NONUNION ( 6 FDA reports)
GROIN PAIN ( 6 FDA reports)
HEAD INJURY ( 6 FDA reports)
IMPAIRED WORK ABILITY ( 6 FDA reports)
MOBILITY DECREASED ( 6 FDA reports)
MUSCLE SPASMS ( 6 FDA reports)
MUSCULAR WEAKNESS ( 6 FDA reports)
NEUROPATHY PERIPHERAL ( 6 FDA reports)
OSTEOARTHRITIS ( 6 FDA reports)
OSTEOPOROTIC FRACTURE ( 6 FDA reports)
PATHOLOGICAL FRACTURE ( 6 FDA reports)
PHOTOSENSITIVITY REACTION ( 6 FDA reports)
PYREXIA ( 6 FDA reports)
SPEECH DISORDER ( 6 FDA reports)
STRESS FRACTURE ( 6 FDA reports)
URTICARIA ( 6 FDA reports)
ANHEDONIA ( 5 FDA reports)
BLOOD CREATININE INCREASED ( 5 FDA reports)
BODY HEIGHT DECREASED ( 5 FDA reports)
CARDIAC DISORDER ( 5 FDA reports)
CONDITION AGGRAVATED ( 5 FDA reports)
DYSARTHRIA ( 5 FDA reports)
FEAR ( 5 FDA reports)
FLATULENCE ( 5 FDA reports)
FLUSHING ( 5 FDA reports)
GALLBLADDER INJURY ( 5 FDA reports)
HAEMATEMESIS ( 5 FDA reports)
HAEMATOCHEZIA ( 5 FDA reports)
HEPATITIS ( 5 FDA reports)
INTENTIONAL DRUG MISUSE ( 5 FDA reports)
MENORRHAGIA ( 5 FDA reports)
MENTAL DISORDER ( 5 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 5 FDA reports)
NECK PAIN ( 5 FDA reports)
NIGHTMARE ( 5 FDA reports)
OFF LABEL USE ( 5 FDA reports)
OVARIAN CYST ( 5 FDA reports)
PAROSMIA ( 5 FDA reports)
PHARYNGEAL OEDEMA ( 5 FDA reports)
PLEURITIC PAIN ( 5 FDA reports)
PRECANCEROUS CELLS PRESENT ( 5 FDA reports)
RESPIRATORY TRACT INFECTION ( 5 FDA reports)
ROAD TRAFFIC ACCIDENT ( 5 FDA reports)
VAGINAL HAEMORRHAGE ( 5 FDA reports)
ABORTION SPONTANEOUS ( 4 FDA reports)
ANGINA UNSTABLE ( 4 FDA reports)
ARTERIOSPASM CORONARY ( 4 FDA reports)
ARTHRITIS ( 4 FDA reports)
BONE GRAFT ( 4 FDA reports)
BURNING SENSATION ( 4 FDA reports)
CHROMATURIA ( 4 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 4 FDA reports)
CRYING ( 4 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 4 FDA reports)
DIFFICULTY IN WALKING ( 4 FDA reports)
EFFUSION ( 4 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 4 FDA reports)
EOSINOPHILIA ( 4 FDA reports)
EXOSTOSIS ( 4 FDA reports)
FACIAL PALSY ( 4 FDA reports)
GAIT DISTURBANCE ( 4 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 4 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 4 FDA reports)
HYPERGLYCAEMIA ( 4 FDA reports)
HYPOTHYROIDISM ( 4 FDA reports)
LIVER DISORDER ( 4 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 4 FDA reports)
MASS ( 4 FDA reports)
MEDICATION ERROR ( 4 FDA reports)
MENSTRUATION IRREGULAR ( 4 FDA reports)
MUSCLE TWITCHING ( 4 FDA reports)
MUSCULOSKELETAL PAIN ( 4 FDA reports)
NERVOUS SYSTEM DISORDER ( 4 FDA reports)
NERVOUSNESS ( 4 FDA reports)
OBESITY ( 4 FDA reports)
OCULAR ICTERUS ( 4 FDA reports)
PHOTOPSIA ( 4 FDA reports)
POOR QUALITY SLEEP ( 4 FDA reports)
PRESYNCOPE ( 4 FDA reports)
RETCHING ( 4 FDA reports)
SEROTONIN SYNDROME ( 4 FDA reports)
SNORING ( 4 FDA reports)
SYNOVIAL CYST ( 4 FDA reports)
AGITATION ( 3 FDA reports)
APHASIA ( 3 FDA reports)
ASTHMA ( 3 FDA reports)
BLINDNESS TRANSIENT ( 3 FDA reports)
BLOOD URINE PRESENT ( 3 FDA reports)
BRAIN NEOPLASM ( 3 FDA reports)
BRONCHITIS ( 3 FDA reports)
BURSITIS ( 3 FDA reports)
CARDIOMYOPATHY ( 3 FDA reports)
CELLULITIS ( 3 FDA reports)
CEREBROVASCULAR SPASM ( 3 FDA reports)
CHILLS ( 3 FDA reports)
CLOSTRIDIAL INFECTION ( 3 FDA reports)
COW'S MILK INTOLERANCE ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
DROOLING ( 3 FDA reports)
DRUG ABUSER ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
ECONOMIC PROBLEM ( 3 FDA reports)
EPISTAXIS ( 3 FDA reports)
EXTRASYSTOLES ( 3 FDA reports)
EYE INFLAMMATION ( 3 FDA reports)
EYE PAIN ( 3 FDA reports)
FACIAL SPASM ( 3 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 3 FDA reports)
GASTRIC DISORDER ( 3 FDA reports)
GASTROINTESTINAL DISORDER ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
GRAND MAL CONVULSION ( 3 FDA reports)
HEPATIC ENZYME INCREASED ( 3 FDA reports)
HEPATIC STEATOSIS ( 3 FDA reports)
HIP DEFORMITY ( 3 FDA reports)
HYPERKALAEMIA ( 3 FDA reports)
HYPERSOMNIA ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
INJECTION SITE HAEMORRHAGE ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 3 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 3 FDA reports)
IRRITABLE BOWEL SYNDROME ( 3 FDA reports)
MIDDLE EAR EFFUSION ( 3 FDA reports)
MOOD ALTERED ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE ( 3 FDA reports)
MULTIPLE SCLEROSIS ( 3 FDA reports)
MUSCLE HAEMORRHAGE ( 3 FDA reports)
MUSCLE RUPTURE ( 3 FDA reports)
MUSCLE TIGHTNESS ( 3 FDA reports)
MYCOBACTERIAL INFECTION ( 3 FDA reports)
NEURALGIA ( 3 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 3 FDA reports)
OVERDOSE ( 3 FDA reports)
PARALYSIS ( 3 FDA reports)
PATHOLOGICAL GAMBLING ( 3 FDA reports)
PNEUMONIA MYCOPLASMAL ( 3 FDA reports)
POSTOPERATIVE INFECTION ( 3 FDA reports)
PROCTOCOLITIS ( 3 FDA reports)
PULMONARY HYPERTENSION ( 3 FDA reports)
RASH GENERALISED ( 3 FDA reports)
RENAL PAIN ( 3 FDA reports)
RESPIRATORY DISTRESS ( 3 FDA reports)
SHOULDER PAIN ( 3 FDA reports)
SLEEP DISORDER ( 3 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
TENDONITIS ( 3 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 3 FDA reports)
THROMBOSIS ( 3 FDA reports)
TOOTH DISORDER ( 3 FDA reports)
TYPE 2 DIABETES MELLITUS ( 3 FDA reports)
VIRAL INFECTION ( 3 FDA reports)
VISUAL DISTURBANCE ( 3 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
ACUTE SINUSITIS ( 2 FDA reports)
ADRENAL HAEMORRHAGE ( 2 FDA reports)
ADVERSE EVENT ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
ALCOHOL USE ( 2 FDA reports)
ANAEMIA POSTOPERATIVE ( 2 FDA reports)
ANKLE FRACTURE ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 2 FDA reports)
BILIARY DYSKINESIA ( 2 FDA reports)
BIPOLAR DISORDER ( 2 FDA reports)
BLADDER DYSFUNCTION ( 2 FDA reports)
BLINDNESS ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BLOOD VISCOSITY INCREASED ( 2 FDA reports)
BRAIN INJURY ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 2 FDA reports)
CANDIDIASIS ( 2 FDA reports)
CARDIAC ANEURYSM ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CEREBRAL ISCHAEMIA ( 2 FDA reports)
CEREBRAL THROMBOSIS ( 2 FDA reports)
CHOKING ( 2 FDA reports)
CLONIC CONVULSION ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
COLITIS ISCHAEMIC ( 2 FDA reports)
COLITIS ULCERATIVE ( 2 FDA reports)
COLOUR BLINDNESS ACQUIRED ( 2 FDA reports)
COORDINATION ABNORMAL ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
CYST ( 2 FDA reports)
DENTAL TREATMENT ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DIABETIC COMA ( 2 FDA reports)
DILATATION VENTRICULAR ( 2 FDA reports)
DIPLOPIA ( 2 FDA reports)
DIVERTICULUM ( 2 FDA reports)
DRUG ABUSE ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
DRUG SCREEN POSITIVE ( 2 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 2 FDA reports)
EMBOLIC STROKE ( 2 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
EYELID PTOSIS ( 2 FDA reports)
FOOD POISONING ( 2 FDA reports)
GASTROINTESTINAL ULCER ( 2 FDA reports)
GASTROOESOPHAGEAL SPHINCTER INSUFFICIENCY ( 2 FDA reports)
GENERALISED ANXIETY DISORDER ( 2 FDA reports)
GENERALISED ERYTHEMA ( 2 FDA reports)
GINGIVITIS ( 2 FDA reports)
GRANULOMA ( 2 FDA reports)
HAEMANGIOMA ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HIATUS HERNIA ( 2 FDA reports)
HIP FRACTURE ( 2 FDA reports)
HYPERCOAGULATION ( 2 FDA reports)
HYPERVENTILATION ( 2 FDA reports)
HYSTERECTOMY ( 2 FDA reports)
INCOHERENT ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
INJECTION SITE HAEMATOMA ( 2 FDA reports)
INJECTION SITE INFECTION ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
INJECTION SITE REACTION ( 2 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 2 FDA reports)
ISCHAEMIC STROKE ( 2 FDA reports)
JOINT SPRAIN ( 2 FDA reports)
LACERATION ( 2 FDA reports)
LIP SWELLING ( 2 FDA reports)
LOCALISED INFECTION ( 2 FDA reports)
LOCALISED OEDEMA ( 2 FDA reports)
MAJOR DEPRESSION ( 2 FDA reports)
MALLORY-WEISS SYNDROME ( 2 FDA reports)
MENISCUS LESION ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 2 FDA reports)
MULTIPLE FRACTURES ( 2 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 2 FDA reports)
MUSCLE DISORDER ( 2 FDA reports)
MUSCLE SPASTICITY ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
NEUROLOGICAL SYMPTOM ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
NON-CARDIAC CHEST PAIN ( 2 FDA reports)
OESOPHAGITIS ( 2 FDA reports)
ORAL CANDIDIASIS ( 2 FDA reports)
OSTEOLYSIS ( 2 FDA reports)
OSTEONECROSIS ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
PANIC ATTACK ( 2 FDA reports)
PANIC DISORDER ( 2 FDA reports)
PANIC REACTION ( 2 FDA reports)
PARTIAL SEIZURES ( 2 FDA reports)
PELVIC VENOUS THROMBOSIS ( 2 FDA reports)
PERIORBITAL OEDEMA ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
PITTING OEDEMA ( 2 FDA reports)
POLYP ( 2 FDA reports)
POOR PERIPHERAL CIRCULATION ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
PSEUDOMONAS INFECTION ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
RIB FRACTURE ( 2 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 2 FDA reports)
SENSORY DISTURBANCE ( 2 FDA reports)
SMEAR CERVIX ABNORMAL ( 2 FDA reports)
SPINAL FRACTURE ( 2 FDA reports)
SPINAL OSTEOARTHRITIS ( 2 FDA reports)
STATUS ASTHMATICUS ( 2 FDA reports)
STOMACH DISCOMFORT ( 2 FDA reports)
STRESS ( 2 FDA reports)
STRESS SYMPTOMS ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
SUNBURN ( 2 FDA reports)
SWELLING ( 2 FDA reports)
TENDON OPERATION ( 2 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 2 FDA reports)
TONSILLECTOMY ( 2 FDA reports)
TOOTH LOSS ( 2 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 2 FDA reports)
TYPE 1 DIABETES MELLITUS ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
URINARY TRACT DISORDER ( 2 FDA reports)
URINE ODOUR ABNORMAL ( 2 FDA reports)
UTERINE DILATION AND CURETTAGE ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
VITAMIN B12 DECREASED ( 2 FDA reports)
VOMITING PROJECTILE ( 2 FDA reports)
WEIGHT ABNORMAL ( 2 FDA reports)
WHEEZING ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
WHITE BLOOD CELL DISORDER ( 2 FDA reports)
ABDOMINAL HERNIA ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ABSCESS LIMB ( 1 FDA reports)
ACCIDENTAL POISONING ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ADENOIDAL HYPERTROPHY ( 1 FDA reports)
ADJUSTMENT DISORDER ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
ALCOHOL ABUSE ( 1 FDA reports)
AMENORRHOEA ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANGER ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANXIETY DISORDER ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
AORTIC VALVE REPLACEMENT ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
APPENDICITIS PERFORATED ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTHROPOD BITE ( 1 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 1 FDA reports)
ATHEROSCLEROSIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
AURA ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BAND SENSATION ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BONE DENSITY DECREASED ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BREAKTHROUGH PAIN ( 1 FDA reports)
BREAST TENDERNESS ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 1 FDA reports)
CARDIOSPASM ( 1 FDA reports)
CAROTID ARTERY DISEASE ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CEREBELLAR ATAXIA ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL CYST ( 1 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CERVICAL DYSPLASIA ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CLUSTER HEADACHE ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
COMPRESSION FRACTURE ( 1 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 1 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 1 FDA reports)
CRUSH INJURY ( 1 FDA reports)
CUBITAL TUNNEL SYNDROME ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DENTAL DISCOMFORT ( 1 FDA reports)
DEPENDENT PERSONALITY DISORDER ( 1 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 1 FDA reports)
DIABETIC GASTROPARESIS ( 1 FDA reports)
DIABETIC NEPHROPATHY ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG SCREEN ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DRY THROAT ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
DYSTHYMIC DISORDER ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EARLY SATIETY ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
ELEVATED MOOD ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ENDODONTIC PROCEDURE ( 1 FDA reports)
ENDOMETRIOSIS ( 1 FDA reports)
ENURESIS ( 1 FDA reports)
EPICONDYLITIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
EYELID DISORDER ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FACIAL DYSMORPHISM ( 1 FDA reports)
FACIAL NERVE DISORDER ( 1 FDA reports)
FEAR OF DEATH ( 1 FDA reports)
FEAR OF DISEASE ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FEMORAL NECK FRACTURE ( 1 FDA reports)
FIBROMUSCULAR DYSPLASIA ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FOOD CRAVING ( 1 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 1 FDA reports)
FOREIGN BODY TRAUMA ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
FRACTURE DELAYED UNION ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
FUNGAL SKIN INFECTION ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GENITAL INFECTION FUNGAL ( 1 FDA reports)
GESTATIONAL DIABETES ( 1 FDA reports)
GINGIVAL ABSCESS ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
GLYCOSURIA ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMOGLOBIN ABNORMAL ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HAEMORRHAGIC OVARIAN CYST ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HAND FRACTURE ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HOMICIDAL IDEATION ( 1 FDA reports)
HUNGER ( 1 FDA reports)
HYPEREMESIS GRAVIDARUM ( 1 FDA reports)
HYPERPYREXIA ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
ILEUS ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFUSION SITE PAIN ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTESTINAL INFARCTION ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
INTESTINAL POLYP ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
JOINT LOCK ( 1 FDA reports)
JOINT SURGERY ( 1 FDA reports)
JUGULAR VEIN THROMBOSIS ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LOSS OF CONTROL OF LEGS ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LOWER EXTREMITY MASS ( 1 FDA reports)
MASKED FACIES ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENSTRUAL DISORDER ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
MITRAL VALVE PROLAPSE ( 1 FDA reports)
MONOPARESIS ( 1 FDA reports)
MOTION SICKNESS ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MUCOSAL EXFOLIATION ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MULTIPLE INJURIES ( 1 FDA reports)
MUSCLE INJURY ( 1 FDA reports)
MUSCLE STRAIN ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
NAIL DISORDER ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NERVE COMPRESSION ( 1 FDA reports)
NERVE INJURY ( 1 FDA reports)
NEUROPATHIC PAIN ( 1 FDA reports)
NON-ALCOHOLIC STEATOHEPATITIS ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OCULAR VASCULAR DISORDER ( 1 FDA reports)
OESOPHAGEAL DISORDER ( 1 FDA reports)
OESOPHAGEAL RUPTURE ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
OSTEOGENESIS IMPERFECTA ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
OTITIS MEDIA ( 1 FDA reports)
OVERWEIGHT ( 1 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 1 FDA reports)
PELVIC PAIN ( 1 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PETIT MAL EPILEPSY ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POOR VENOUS ACCESS ( 1 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PRINZMETAL ANGINA ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PSYCHOLOGICAL TRAUMA ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
RAYNAUD'S PHENOMENON ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SCAR ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SENSATION OF PRESSURE ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN INDURATION ( 1 FDA reports)
SKIN MASS ( 1 FDA reports)
SKIN ODOUR ABNORMAL ( 1 FDA reports)
SLEEP WALKING ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SOMATOFORM DISORDER ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
TENSION HEADACHE ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THIRST ( 1 FDA reports)
THORACIC OUTLET SYNDROME ( 1 FDA reports)
THYROXINE INCREASED ( 1 FDA reports)
TINEA PEDIS ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO INCREASED ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TRI-IODOTHYRONINE INCREASED ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
UMBILICAL HERNIA ( 1 FDA reports)
UNEMPLOYMENT ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINE OUTPUT INCREASED ( 1 FDA reports)
UTERINE LEIOMYOMA ( 1 FDA reports)
UTERINE POLYP ( 1 FDA reports)
VAGINAL INFECTION ( 1 FDA reports)
VASOCONSTRICTION ( 1 FDA reports)
VENOUS THROMBOSIS ( 1 FDA reports)
VENOUS VALVE RUPTURED ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VOCAL CORD DISORDER ( 1 FDA reports)
VULVAL DISORDER ( 1 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WOUND DEHISCENCE ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use