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

DEPRESSION ( 250 FDA reports)
NAUSEA ( 179 FDA reports)
ANXIETY ( 142 FDA reports)
FATIGUE ( 142 FDA reports)
DYSPNOEA ( 127 FDA reports)
VOMITING ( 116 FDA reports)
PAIN ( 109 FDA reports)
DRUG INEFFECTIVE ( 108 FDA reports)
FALL ( 106 FDA reports)
FEELING ABNORMAL ( 104 FDA reports)
HEADACHE ( 103 FDA reports)
DIARRHOEA ( 98 FDA reports)
SUICIDAL IDEATION ( 98 FDA reports)
DIZZINESS ( 95 FDA reports)
MALAISE ( 95 FDA reports)
WEIGHT DECREASED ( 89 FDA reports)
INSOMNIA ( 88 FDA reports)
ASTHENIA ( 83 FDA reports)
GAIT DISTURBANCE ( 75 FDA reports)
SOMNOLENCE ( 74 FDA reports)
CONFUSIONAL STATE ( 69 FDA reports)
WEIGHT INCREASED ( 69 FDA reports)
OVERDOSE ( 68 FDA reports)
SUICIDE ATTEMPT ( 68 FDA reports)
PNEUMONIA ( 62 FDA reports)
ABDOMINAL PAIN ( 61 FDA reports)
ARTHRALGIA ( 61 FDA reports)
PAIN IN EXTREMITY ( 61 FDA reports)
LOSS OF CONSCIOUSNESS ( 58 FDA reports)
CONVULSION ( 57 FDA reports)
OEDEMA PERIPHERAL ( 57 FDA reports)
DEATH ( 56 FDA reports)
HYPERTENSION ( 56 FDA reports)
PARAESTHESIA ( 56 FDA reports)
TREMOR ( 54 FDA reports)
HYPOTENSION ( 51 FDA reports)
HYPERHIDROSIS ( 49 FDA reports)
BLOOD GLUCOSE INCREASED ( 47 FDA reports)
COMPLETED SUICIDE ( 47 FDA reports)
AGITATION ( 46 FDA reports)
CHEST PAIN ( 46 FDA reports)
BACK PAIN ( 45 FDA reports)
DRUG INTERACTION ( 45 FDA reports)
CONSTIPATION ( 43 FDA reports)
CONDITION AGGRAVATED ( 42 FDA reports)
COUGH ( 39 FDA reports)
MOOD SWINGS ( 39 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 37 FDA reports)
PRURITUS ( 37 FDA reports)
BLOOD PRESSURE INCREASED ( 36 FDA reports)
DRUG DEPENDENCE ( 36 FDA reports)
PYREXIA ( 36 FDA reports)
ABNORMAL BEHAVIOUR ( 35 FDA reports)
CEREBROVASCULAR ACCIDENT ( 35 FDA reports)
DECREASED APPETITE ( 34 FDA reports)
HALLUCINATION ( 34 FDA reports)
DRY MOUTH ( 33 FDA reports)
INJURY ( 33 FDA reports)
RASH ( 33 FDA reports)
SYNCOPE ( 33 FDA reports)
MEMORY IMPAIRMENT ( 32 FDA reports)
PULMONARY OEDEMA ( 32 FDA reports)
RENAL FAILURE ( 30 FDA reports)
BALANCE DISORDER ( 29 FDA reports)
HYPERSENSITIVITY ( 29 FDA reports)
NIGHTMARE ( 29 FDA reports)
URTICARIA ( 29 FDA reports)
ABDOMINAL DISTENSION ( 28 FDA reports)
AGGRESSION ( 28 FDA reports)
CONTUSION ( 28 FDA reports)
ERYTHEMA ( 28 FDA reports)
INTENTIONAL OVERDOSE ( 28 FDA reports)
MYALGIA ( 28 FDA reports)
OSTEOARTHRITIS ( 28 FDA reports)
PALPITATIONS ( 28 FDA reports)
STRESS ( 28 FDA reports)
VISION BLURRED ( 28 FDA reports)
INJECTION SITE PAIN ( 27 FDA reports)
AMNESIA ( 26 FDA reports)
BRONCHITIS ( 26 FDA reports)
DEHYDRATION ( 26 FDA reports)
HEART RATE INCREASED ( 26 FDA reports)
MUSCLE SPASMS ( 26 FDA reports)
NERVOUSNESS ( 26 FDA reports)
ABDOMINAL PAIN UPPER ( 25 FDA reports)
ABNORMAL DREAMS ( 25 FDA reports)
ANGINA PECTORIS ( 25 FDA reports)
CARDIAC FAILURE ( 25 FDA reports)
CHEST DISCOMFORT ( 25 FDA reports)
INFLUENZA LIKE ILLNESS ( 25 FDA reports)
PANIC ATTACK ( 25 FDA reports)
URINARY TRACT INFECTION ( 25 FDA reports)
ANAEMIA ( 24 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 24 FDA reports)
BLOOD CREATININE INCREASED ( 24 FDA reports)
CHILLS ( 24 FDA reports)
HYPOAESTHESIA ( 24 FDA reports)
PARANOIA ( 24 FDA reports)
PSYCHOTIC DISORDER ( 24 FDA reports)
CRYING ( 23 FDA reports)
DEPRESSED MOOD ( 23 FDA reports)
MUSCULAR WEAKNESS ( 23 FDA reports)
SLEEP DISORDER ( 23 FDA reports)
UNRESPONSIVE TO STIMULI ( 23 FDA reports)
DRUG DOSE OMISSION ( 22 FDA reports)
DYSGEUSIA ( 22 FDA reports)
FLUSHING ( 22 FDA reports)
MENTAL DISORDER ( 22 FDA reports)
MITRAL VALVE INCOMPETENCE ( 22 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 22 FDA reports)
NECK PAIN ( 22 FDA reports)
OFF LABEL USE ( 22 FDA reports)
RESPIRATORY FAILURE ( 22 FDA reports)
ROAD TRAFFIC ACCIDENT ( 22 FDA reports)
ABDOMINAL DISCOMFORT ( 21 FDA reports)
CARDIAC ARREST ( 21 FDA reports)
DIABETES MELLITUS ( 21 FDA reports)
VISUAL IMPAIRMENT ( 21 FDA reports)
ANGER ( 20 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 20 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 20 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 20 FDA reports)
IRRITABILITY ( 20 FDA reports)
LETHARGY ( 20 FDA reports)
MEDICATION ERROR ( 20 FDA reports)
PULMONARY EMBOLISM ( 20 FDA reports)
TOOTH LOSS ( 20 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 20 FDA reports)
ACCIDENTAL OVERDOSE ( 19 FDA reports)
ALOPECIA ( 19 FDA reports)
ATRIAL FIBRILLATION ( 19 FDA reports)
BLOOD PRESSURE DECREASED ( 19 FDA reports)
CORONARY ARTERY DISEASE ( 19 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 19 FDA reports)
HAEMOGLOBIN DECREASED ( 19 FDA reports)
INTENTIONAL DRUG MISUSE ( 19 FDA reports)
MULTIPLE SCLEROSIS ( 19 FDA reports)
MYOCARDIAL INFARCTION ( 19 FDA reports)
NEUROPATHY PERIPHERAL ( 19 FDA reports)
COMA ( 18 FDA reports)
CROHN'S DISEASE ( 18 FDA reports)
DRUG HYPERSENSITIVITY ( 18 FDA reports)
HYPOGLYCAEMIA ( 18 FDA reports)
HYPONATRAEMIA ( 18 FDA reports)
MENTAL IMPAIRMENT ( 18 FDA reports)
PANCREATITIS ( 18 FDA reports)
RENAL DISORDER ( 18 FDA reports)
TACHYCARDIA ( 18 FDA reports)
THROMBOSIS ( 18 FDA reports)
CARDIOMEGALY ( 17 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 17 FDA reports)
DISORIENTATION ( 17 FDA reports)
DRUG TOXICITY ( 17 FDA reports)
FEELING HOT ( 17 FDA reports)
INCORRECT DOSE ADMINISTERED ( 17 FDA reports)
PULMONARY HYPERTENSION ( 17 FDA reports)
SKIN DISCOLOURATION ( 17 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 16 FDA reports)
BREAST CANCER ( 16 FDA reports)
DEEP VEIN THROMBOSIS ( 16 FDA reports)
DELUSION ( 16 FDA reports)
DYSARTHRIA ( 16 FDA reports)
EMOTIONAL DISTRESS ( 16 FDA reports)
HEPATIC STEATOSIS ( 16 FDA reports)
HOSPITALISATION ( 16 FDA reports)
HOT FLUSH ( 16 FDA reports)
MOBILITY DECREASED ( 16 FDA reports)
OEDEMA ( 16 FDA reports)
ARTHRITIS ( 15 FDA reports)
ASTHMA ( 15 FDA reports)
BONE DISORDER ( 15 FDA reports)
DISTURBANCE IN ATTENTION ( 15 FDA reports)
DYSURIA ( 15 FDA reports)
GLAUCOMA ( 15 FDA reports)
HYPERGLYCAEMIA ( 15 FDA reports)
HYPOKALAEMIA ( 15 FDA reports)
JAW FRACTURE ( 15 FDA reports)
MULTIPLE DRUG OVERDOSE ( 15 FDA reports)
OSTEONECROSIS OF JAW ( 15 FDA reports)
PLEURAL EFFUSION ( 15 FDA reports)
RENAL FAILURE ACUTE ( 15 FDA reports)
SEDATION ( 15 FDA reports)
SEPSIS ( 15 FDA reports)
SKIN LESION ( 15 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 15 FDA reports)
SWELLING FACE ( 15 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 15 FDA reports)
WITHDRAWAL SYNDROME ( 15 FDA reports)
BIPOLAR DISORDER ( 14 FDA reports)
DELIRIUM ( 14 FDA reports)
ECZEMA ( 14 FDA reports)
HAEMORRHAGE ( 14 FDA reports)
HYPERSOMNIA ( 14 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 14 FDA reports)
INJECTION SITE ERYTHEMA ( 14 FDA reports)
IRRITABLE BOWEL SYNDROME ( 14 FDA reports)
LIBIDO DECREASED ( 14 FDA reports)
LYMPHADENOPATHY ( 14 FDA reports)
MOLE EXCISION ( 14 FDA reports)
OBESITY ( 14 FDA reports)
SPEECH DISORDER ( 14 FDA reports)
SWELLING ( 14 FDA reports)
TOOTH EXTRACTION ( 14 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 14 FDA reports)
UNEVALUABLE EVENT ( 14 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 14 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 14 FDA reports)
ABASIA ( 13 FDA reports)
BEDRIDDEN ( 13 FDA reports)
BLINDNESS UNILATERAL ( 13 FDA reports)
COGNITIVE DISORDER ( 13 FDA reports)
DRUG EFFECT DECREASED ( 13 FDA reports)
DYSPHONIA ( 13 FDA reports)
FLATULENCE ( 13 FDA reports)
HEAD INJURY ( 13 FDA reports)
IMPAIRED HEALING ( 13 FDA reports)
IMPAIRED WORK ABILITY ( 13 FDA reports)
INFLUENZA ( 13 FDA reports)
PRODUCT QUALITY ISSUE ( 13 FDA reports)
PSORIASIS ( 13 FDA reports)
SEROTONIN SYNDROME ( 13 FDA reports)
SNEEZING ( 13 FDA reports)
VISUAL ACUITY REDUCED ( 13 FDA reports)
APATHY ( 12 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 12 FDA reports)
GASTROENTERITIS RADIATION ( 12 FDA reports)
INCONTINENCE ( 12 FDA reports)
JAW DISORDER ( 12 FDA reports)
LEFT ATRIAL DILATATION ( 12 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 12 FDA reports)
NEPHROLITHIASIS ( 12 FDA reports)
OSTEOMYELITIS ( 12 FDA reports)
RENAL IMPAIRMENT ( 12 FDA reports)
ATAXIA ( 11 FDA reports)
BLADDER MASS ( 11 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 11 FDA reports)
CARDIAC DISORDER ( 11 FDA reports)
CEREBRAL HAEMORRHAGE ( 11 FDA reports)
CYSTITIS ( 11 FDA reports)
DRY EYE ( 11 FDA reports)
DYSPHAGIA ( 11 FDA reports)
EUPHORIC MOOD ( 11 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 11 FDA reports)
ILL-DEFINED DISORDER ( 11 FDA reports)
LUNG INFILTRATION ( 11 FDA reports)
MANIA ( 11 FDA reports)
METASTATIC NEOPLASM ( 11 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 11 FDA reports)
NO ADVERSE EVENT ( 11 FDA reports)
PARALYSIS ( 11 FDA reports)
RASH PRURITIC ( 11 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 11 FDA reports)
TREATMENT NONCOMPLIANCE ( 11 FDA reports)
WHEEZING ( 11 FDA reports)
ACCIDENTAL EXPOSURE ( 10 FDA reports)
ACTINIC KERATOSIS ( 10 FDA reports)
ADVERSE EVENT ( 10 FDA reports)
ANOREXIA ( 10 FDA reports)
AORTIC VALVE STENOSIS ( 10 FDA reports)
APHASIA ( 10 FDA reports)
BLINDNESS ( 10 FDA reports)
BREAST LUMP REMOVAL ( 10 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 10 FDA reports)
CATARACT ( 10 FDA reports)
CERVICAL CYST ( 10 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 10 FDA reports)
DERMATITIS ( 10 FDA reports)
DISABILITY ( 10 FDA reports)
DRUG ABUSER ( 10 FDA reports)
DRUG ERUPTION ( 10 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 10 FDA reports)
DRUG INTOLERANCE ( 10 FDA reports)
DRUG SCREEN POSITIVE ( 10 FDA reports)
DYSPLASTIC NAEVUS SYNDROME ( 10 FDA reports)
EYE SWELLING ( 10 FDA reports)
FEAR ( 10 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 10 FDA reports)
FIBROMYALGIA ( 10 FDA reports)
HALLUCINATION, VISUAL ( 10 FDA reports)
HEART RATE IRREGULAR ( 10 FDA reports)
HODGKIN'S DISEASE ( 10 FDA reports)
HYSTERECTOMY ( 10 FDA reports)
INTENTIONAL SELF-INJURY ( 10 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 10 FDA reports)
KYPHOSCOLIOSIS ( 10 FDA reports)
LYMPHADENECTOMY ( 10 FDA reports)
MOOD ALTERED ( 10 FDA reports)
MOVEMENT DISORDER ( 10 FDA reports)
NERVOUS SYSTEM DISORDER ( 10 FDA reports)
PANIC REACTION ( 10 FDA reports)
PARKINSONISM ( 10 FDA reports)
SEBORRHOEIC KERATOSIS ( 10 FDA reports)
SKIN FIBROSIS ( 10 FDA reports)
SKIN PAPILLOMA ( 10 FDA reports)
SUBSTANCE ABUSE ( 10 FDA reports)
VERTIGO ( 10 FDA reports)
ADVERSE DRUG REACTION ( 9 FDA reports)
APPENDICECTOMY ( 9 FDA reports)
BLOOD POTASSIUM DECREASED ( 9 FDA reports)
DEMENTIA ( 9 FDA reports)
EATING DISORDER ( 9 FDA reports)
EYE DISORDER ( 9 FDA reports)
GALLBLADDER DISORDER ( 9 FDA reports)
GASTROINTESTINAL DISORDER ( 9 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 9 FDA reports)
HAEMATOCHEZIA ( 9 FDA reports)
HALLUCINATION, AUDITORY ( 9 FDA reports)
HERPES ZOSTER ( 9 FDA reports)
IMPAIRED DRIVING ABILITY ( 9 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 9 FDA reports)
INJECTION SITE HAEMATOMA ( 9 FDA reports)
INJECTION SITE HAEMORRHAGE ( 9 FDA reports)
LUNG DISORDER ( 9 FDA reports)
OXYGEN SATURATION DECREASED ( 9 FDA reports)
PNEUMONIA ASPIRATION ( 9 FDA reports)
RESPIRATORY ARREST ( 9 FDA reports)
RESTLESSNESS ( 9 FDA reports)
SKIN LACERATION ( 9 FDA reports)
SUICIDAL BEHAVIOUR ( 9 FDA reports)
THROAT IRRITATION ( 9 FDA reports)
ACUTE SINUSITIS ( 8 FDA reports)
ATELECTASIS ( 8 FDA reports)
ATROPHIC VULVOVAGINITIS ( 8 FDA reports)
AURICULAR PSEUDOCYST ( 8 FDA reports)
CYANOSIS ( 8 FDA reports)
DEBRIDEMENT ( 8 FDA reports)
DECREASED INTEREST ( 8 FDA reports)
DYSKINESIA ( 8 FDA reports)
DYSPNOEA EXERTIONAL ( 8 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 8 FDA reports)
ENDOTRACHEAL INTUBATION ( 8 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 8 FDA reports)
HYPERTENSIVE CRISIS ( 8 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 8 FDA reports)
INTERTRIGO ( 8 FDA reports)
MENSTRUATION IRREGULAR ( 8 FDA reports)
MIDDLE INSOMNIA ( 8 FDA reports)
MUSCLE INJURY ( 8 FDA reports)
NASAL CONGESTION ( 8 FDA reports)
NASOPHARYNGITIS ( 8 FDA reports)
OOPHORECTOMY ( 8 FDA reports)
PALLOR ( 8 FDA reports)
PLANTAR FASCIITIS ( 8 FDA reports)
PLATELET COUNT DECREASED ( 8 FDA reports)
POISONING ( 8 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 8 FDA reports)
PULMONARY FIBROSIS ( 8 FDA reports)
RESPIRATORY DEPRESSION ( 8 FDA reports)
RESPIRATORY DISORDER ( 8 FDA reports)
SENSATION OF HEAVINESS ( 8 FDA reports)
SKIN OEDEMA ( 8 FDA reports)
SPINAL FRACTURE ( 8 FDA reports)
TENDONITIS ( 8 FDA reports)
THERAPEUTIC PROCEDURE ( 8 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 8 FDA reports)
THINKING ABNORMAL ( 8 FDA reports)
ULTRASOUND PELVIS ABNORMAL ( 8 FDA reports)
URINE CYTOLOGY ABNORMAL ( 8 FDA reports)
AMENORRHOEA ( 7 FDA reports)
APPARENT DEATH ( 7 FDA reports)
ARRHYTHMIA ( 7 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 7 FDA reports)
BASAL CELL CARCINOMA ( 7 FDA reports)
BLADDER DISORDER ( 7 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 7 FDA reports)
BLOOD MAGNESIUM DECREASED ( 7 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 7 FDA reports)
BLOOD URINE PRESENT ( 7 FDA reports)
BODY TEMPERATURE INCREASED ( 7 FDA reports)
CARDIAC PACEMAKER INSERTION ( 7 FDA reports)
CARDIOMYOPATHY ( 7 FDA reports)
CHOLELITHIASIS ( 7 FDA reports)
COLITIS ( 7 FDA reports)
DEPRESSION SUICIDAL ( 7 FDA reports)
DIPLOPIA ( 7 FDA reports)
DRUG PRESCRIBING ERROR ( 7 FDA reports)
DRY SKIN ( 7 FDA reports)
ENDOCARDITIS ( 7 FDA reports)
EPILEPSY ( 7 FDA reports)
EPISTAXIS ( 7 FDA reports)
ERECTILE DYSFUNCTION ( 7 FDA reports)
FOOT FRACTURE ( 7 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 7 FDA reports)
HEPATIC FAILURE ( 7 FDA reports)
INJECTION SITE PRURITUS ( 7 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 7 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 7 FDA reports)
LIMB INJURY ( 7 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 7 FDA reports)
MOTOR DYSFUNCTION ( 7 FDA reports)
MULTI-ORGAN FAILURE ( 7 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 7 FDA reports)
PERIARTHRITIS ( 7 FDA reports)
PROCEDURAL COMPLICATION ( 7 FDA reports)
PRURITUS GENERALISED ( 7 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 7 FDA reports)
RETCHING ( 7 FDA reports)
SCHIZOPHRENIA ( 7 FDA reports)
SCREAMING ( 7 FDA reports)
SEBORRHOEIC DERMATITIS ( 7 FDA reports)
SINUSITIS ( 7 FDA reports)
STUPOR ( 7 FDA reports)
THROMBOCYTOPENIA ( 7 FDA reports)
VISUAL DISTURBANCE ( 7 FDA reports)
ACUTE RESPIRATORY FAILURE ( 6 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 6 FDA reports)
ANHEDONIA ( 6 FDA reports)
APHAGIA ( 6 FDA reports)
BLOOD UREA INCREASED ( 6 FDA reports)
BONE PAIN ( 6 FDA reports)
CARPAL TUNNEL SYNDROME ( 6 FDA reports)
DEAFNESS ( 6 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 6 FDA reports)
DENTAL CARIES ( 6 FDA reports)
DIABETIC NEUROPATHY ( 6 FDA reports)
DISEASE RECURRENCE ( 6 FDA reports)
DRUG ABUSE ( 6 FDA reports)
DRUG ADMINISTRATION ERROR ( 6 FDA reports)
DYSTONIA ( 6 FDA reports)
EJECTION FRACTION DECREASED ( 6 FDA reports)
EMOTIONAL DISORDER ( 6 FDA reports)
EMPHYSEMA ( 6 FDA reports)
EYE OEDEMA ( 6 FDA reports)
EYE PAIN ( 6 FDA reports)
FEELING COLD ( 6 FDA reports)
FORMICATION ( 6 FDA reports)
GRAND MAL CONVULSION ( 6 FDA reports)
HEAD DISCOMFORT ( 6 FDA reports)
HEARING IMPAIRED ( 6 FDA reports)
HEMICEPHALALGIA ( 6 FDA reports)
HEMIPARESIS ( 6 FDA reports)
HEPATIC ENZYME INCREASED ( 6 FDA reports)
HOMICIDAL IDEATION ( 6 FDA reports)
HYPERAESTHESIA ( 6 FDA reports)
INITIAL INSOMNIA ( 6 FDA reports)
INJECTION SITE REACTION ( 6 FDA reports)
JOINT SWELLING ( 6 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 6 FDA reports)
MACULAR DEGENERATION ( 6 FDA reports)
METASTASES TO BONE ( 6 FDA reports)
NEOPLASM MALIGNANT ( 6 FDA reports)
NEURITIS ( 6 FDA reports)
ONYCHOMYCOSIS ( 6 FDA reports)
PETECHIAE ( 6 FDA reports)
PHARYNGEAL OEDEMA ( 6 FDA reports)
POOR QUALITY SLEEP ( 6 FDA reports)
RECTAL HAEMORRHAGE ( 6 FDA reports)
RENAL FAILURE CHRONIC ( 6 FDA reports)
RIB FRACTURE ( 6 FDA reports)
SINUS DISORDER ( 6 FDA reports)
SINUS TACHYCARDIA ( 6 FDA reports)
STAPHYLOCOCCAL INFECTION ( 6 FDA reports)
TARDIVE DYSKINESIA ( 6 FDA reports)
TIC ( 6 FDA reports)
TINNITUS ( 6 FDA reports)
TYPE 1 DIABETES MELLITUS ( 6 FDA reports)
TYPE 2 DIABETES MELLITUS ( 6 FDA reports)
ACROMEGALY ( 5 FDA reports)
ALCOHOL USE ( 5 FDA reports)
ANAL HAEMORRHAGE ( 5 FDA reports)
ANAPHYLACTIC REACTION ( 5 FDA reports)
BED REST ( 5 FDA reports)
BLINDNESS TRANSIENT ( 5 FDA reports)
BLOOD COUNT ABNORMAL ( 5 FDA reports)
BLOOD GROWTH HORMONE INCREASED ( 5 FDA reports)
BLOOD PROLACTIN INCREASED ( 5 FDA reports)
BOWEL SOUNDS ABNORMAL ( 5 FDA reports)
BREAST CANCER METASTATIC ( 5 FDA reports)
BURNING SENSATION ( 5 FDA reports)
CEREBRAL ATROPHY ( 5 FDA reports)
CLAUSTROPHOBIA ( 5 FDA reports)
DIASTOLIC DYSFUNCTION ( 5 FDA reports)
DIVERTICULUM INTESTINAL ( 5 FDA reports)
DRUG LEVEL INCREASED ( 5 FDA reports)
DYSPHEMIA ( 5 FDA reports)
EAR PAIN ( 5 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 5 FDA reports)
EPICONDYLITIS ( 5 FDA reports)
EXTRASYSTOLES ( 5 FDA reports)
FLUID RETENTION ( 5 FDA reports)
FURUNCLE ( 5 FDA reports)
HAEMATURIA ( 5 FDA reports)
HAIR DISORDER ( 5 FDA reports)
HEART RATE DECREASED ( 5 FDA reports)
HERPES SIMPLEX ( 5 FDA reports)
HYPEREOSINOPHILIC SYNDROME ( 5 FDA reports)
HYPERVIGILANCE ( 5 FDA reports)
INADEQUATE ANALGESIA ( 5 FDA reports)
INCOHERENT ( 5 FDA reports)
INCREASED TENDENCY TO BRUISE ( 5 FDA reports)
INFLAMMATION ( 5 FDA reports)
INFUSION SITE PAIN ( 5 FDA reports)
INSULIN-LIKE GROWTH FACTOR INCREASED ( 5 FDA reports)
LABORATORY TEST ABNORMAL ( 5 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 5 FDA reports)
MAJOR DEPRESSION ( 5 FDA reports)
MALNUTRITION ( 5 FDA reports)
MASS ( 5 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 5 FDA reports)
MUSCLE ATROPHY ( 5 FDA reports)
MYOCLONUS ( 5 FDA reports)
NIGHT SWEATS ( 5 FDA reports)
PARONYCHIA ( 5 FDA reports)
PERICARDIAL EFFUSION ( 5 FDA reports)
PERICARDITIS ( 5 FDA reports)
PERIORBITAL HAEMATOMA ( 5 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 5 FDA reports)
PROTEIN URINE PRESENT ( 5 FDA reports)
QUALITY OF LIFE DECREASED ( 5 FDA reports)
RESPIRATORY DISTRESS ( 5 FDA reports)
RESTLESS LEGS SYNDROME ( 5 FDA reports)
SECRETION DISCHARGE ( 5 FDA reports)
SENSATION OF FOREIGN BODY ( 5 FDA reports)
SKIN BURNING SENSATION ( 5 FDA reports)
SKIN DISORDER ( 5 FDA reports)
SLEEP APNOEA SYNDROME ( 5 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 5 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 5 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 5 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 5 FDA reports)
SURGERY ( 5 FDA reports)
THORACIC CAVITY DRAINAGE ( 5 FDA reports)
ABORTION SPONTANEOUS ( 4 FDA reports)
ACUTE CORONARY SYNDROME ( 4 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 4 FDA reports)
AKATHISIA ( 4 FDA reports)
ANKLE FRACTURE ( 4 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 4 FDA reports)
ARTHROPATHY ( 4 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 4 FDA reports)
BLOOD BILIRUBIN INCREASED ( 4 FDA reports)
BLOOD CALCIUM DECREASED ( 4 FDA reports)
BLOOD POTASSIUM INCREASED ( 4 FDA reports)
BLOOD PRESSURE ABNORMAL ( 4 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 4 FDA reports)
BLOOD SODIUM DECREASED ( 4 FDA reports)
BODY HEIGHT DECREASED ( 4 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 4 FDA reports)
CHONDROSARCOMA ( 4 FDA reports)
CIRCULATORY COLLAPSE ( 4 FDA reports)
COORDINATION ABNORMAL ( 4 FDA reports)
CORONARY ARTERY RESTENOSIS ( 4 FDA reports)
DENTAL NECROSIS ( 4 FDA reports)
DEPRESSIVE SYMPTOM ( 4 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 4 FDA reports)
DIFFICULTY IN WALKING ( 4 FDA reports)
DISEASE PROGRESSION ( 4 FDA reports)
DIVERTICULITIS ( 4 FDA reports)
DRUG DIVERSION ( 4 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 4 FDA reports)
ENDOMETRIOSIS ( 4 FDA reports)
ESCHERICHIA INFECTION ( 4 FDA reports)
EXOPHTHALMOS ( 4 FDA reports)
EYE IRRITATION ( 4 FDA reports)
EYELID OEDEMA ( 4 FDA reports)
FACE OEDEMA ( 4 FDA reports)
FAECES DISCOLOURED ( 4 FDA reports)
FUNGAL INFECTION ( 4 FDA reports)
GALLBLADDER OPERATION ( 4 FDA reports)
GASTRITIS ( 4 FDA reports)
GENERAL SYMPTOM ( 4 FDA reports)
GENITAL HERPES ( 4 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 4 FDA reports)
GUN SHOT WOUND ( 4 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 4 FDA reports)
HEPATITIS ( 4 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 4 FDA reports)
HYPERCHOLESTEROLAEMIA ( 4 FDA reports)
HYPERPHAGIA ( 4 FDA reports)
HYPERVENTILATION ( 4 FDA reports)
HYPOCHONDRIASIS ( 4 FDA reports)
HYPOKINESIA ( 4 FDA reports)
HYPOTHERMIA ( 4 FDA reports)
HYPOTHYROIDISM ( 4 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 4 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 4 FDA reports)
INTENTIONAL MISUSE ( 4 FDA reports)
INTERSTITIAL LUNG DISEASE ( 4 FDA reports)
ISCHAEMIC STROKE ( 4 FDA reports)
JUDGEMENT IMPAIRED ( 4 FDA reports)
LACRIMATION INCREASED ( 4 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 4 FDA reports)
MENTAL STATUS CHANGES ( 4 FDA reports)
METABOLIC DISORDER ( 4 FDA reports)
MIGRAINE ( 4 FDA reports)
MYOPATHY ( 4 FDA reports)
NASAL DISCOMFORT ( 4 FDA reports)
NERVE COMPRESSION ( 4 FDA reports)
NEUTROPHIL COUNT INCREASED ( 4 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 4 FDA reports)
ORAL PAIN ( 4 FDA reports)
OROPHARYNGEAL PAIN ( 4 FDA reports)
ORTHOSTATIC HYPOTENSION ( 4 FDA reports)
PELVIC FRACTURE ( 4 FDA reports)
PHOBIA ( 4 FDA reports)
PREGNANCY ( 4 FDA reports)
PREMATURE BABY ( 4 FDA reports)
PRESYNCOPE ( 4 FDA reports)
PSYCHIATRIC SYMPTOM ( 4 FDA reports)
PULMONARY CONGESTION ( 4 FDA reports)
RASH GENERALISED ( 4 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 4 FDA reports)
RESPIRATORY TRACT INFECTION ( 4 FDA reports)
RHEUMATOID ARTHRITIS ( 4 FDA reports)
ROTATOR CUFF SYNDROME ( 4 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 4 FDA reports)
SENSORY DISTURBANCE ( 4 FDA reports)
SENSORY LOSS ( 4 FDA reports)
SEXUAL DYSFUNCTION ( 4 FDA reports)
SHOCK ( 4 FDA reports)
SKIN INDURATION ( 4 FDA reports)
SKIN MASS ( 4 FDA reports)
SKIN REACTION ( 4 FDA reports)
SKIN ULCER ( 4 FDA reports)
SNORING ( 4 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 4 FDA reports)
TOOTHACHE ( 4 FDA reports)
UNDERDOSE ( 4 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 4 FDA reports)
URINARY INCONTINENCE ( 4 FDA reports)
VAGINAL HAEMORRHAGE ( 4 FDA reports)
VASCULITIS ( 4 FDA reports)
VENTRICULAR FAILURE ( 4 FDA reports)
WOUND ( 4 FDA reports)
XANTHOPSIA ( 4 FDA reports)
ABDOMINAL PAIN LOWER ( 3 FDA reports)
ABDOMINAL WALL ABSCESS ( 3 FDA reports)
ABNORMAL WEIGHT GAIN ( 3 FDA reports)
ABSCESS DRAINAGE ( 3 FDA reports)
ACCIDENT ( 3 FDA reports)
ACUTE HEPATIC FAILURE ( 3 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 3 FDA reports)
AFFECTIVE DISORDER ( 3 FDA reports)
AGEUSIA ( 3 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 3 FDA reports)
ALVEOLITIS ( 3 FDA reports)
ALVEOLITIS ALLERGIC ( 3 FDA reports)
ANAL STENOSIS ( 3 FDA reports)
ANOSMIA ( 3 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 3 FDA reports)
APPENDICITIS ( 3 FDA reports)
APPETITE DISORDER ( 3 FDA reports)
APPLICATION SITE DISCOLOURATION ( 3 FDA reports)
APPLICATION SITE ERYTHEMA ( 3 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 3 FDA reports)
ASCITES ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 3 FDA reports)
BABESIOSIS ( 3 FDA reports)
BIPOLAR I DISORDER ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 3 FDA reports)
BLOOD GLUCOSE DECREASED ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 3 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 3 FDA reports)
BLOOD PROLACTIN ABNORMAL ( 3 FDA reports)
BLOOD TEST ABNORMAL ( 3 FDA reports)
BLOOD TESTOSTERONE ABNORMAL ( 3 FDA reports)
BRADYCARDIA ( 3 FDA reports)
BRAIN HERNIATION ( 3 FDA reports)
BRAIN OEDEMA ( 3 FDA reports)
BREAST CANCER FEMALE ( 3 FDA reports)
BRONCHITIS CHRONIC ( 3 FDA reports)
CALCULUS URETERIC ( 3 FDA reports)
CARBON DIOXIDE INCREASED ( 3 FDA reports)
CEREBRAL INFARCTION ( 3 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 3 FDA reports)
CERVICOBRACHIAL SYNDROME ( 3 FDA reports)
CHOKING ( 3 FDA reports)
DECREASED ACTIVITY ( 3 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 3 FDA reports)
DEVICE RELATED INFECTION ( 3 FDA reports)
DIABETIC RETINOPATHY ( 3 FDA reports)
DIALYSIS ( 3 FDA reports)
DILATATION VENTRICULAR ( 3 FDA reports)
DIVERTICULUM ( 3 FDA reports)
DROOLING ( 3 FDA reports)
DRUG TOLERANCE ( 3 FDA reports)
DYSLALIA ( 3 FDA reports)
DYSMENORRHOEA ( 3 FDA reports)
DYSPEPSIA ( 3 FDA reports)
ENERGY INCREASED ( 3 FDA reports)
EYE HAEMORRHAGE ( 3 FDA reports)
EYE INFECTION ( 3 FDA reports)
FACIAL PAIN ( 3 FDA reports)
FEELING JITTERY ( 3 FDA reports)
FEELING OF DESPAIR ( 3 FDA reports)
FEELINGS OF WORTHLESSNESS ( 3 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 3 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 3 FDA reports)
GASTRIC DISORDER ( 3 FDA reports)
GASTROENTERITIS ( 3 FDA reports)
GASTROENTERITIS VIRAL ( 3 FDA reports)
GENITAL INFECTION FEMALE ( 3 FDA reports)
GINGIVAL DISORDER ( 3 FDA reports)
GLOMERULAR FILTRATION RATE INCREASED ( 3 FDA reports)
GOITRE ( 3 FDA reports)
HEART VALVE OPERATION ( 3 FDA reports)
HERNIA ( 3 FDA reports)
HIP FRACTURE ( 3 FDA reports)
HYDRONEPHROSIS ( 3 FDA reports)
HYPERTHERMIA ( 3 FDA reports)
HYPOAESTHESIA ORAL ( 3 FDA reports)
HYPOGLYCAEMIC COMA ( 3 FDA reports)
HYPOPHAGIA ( 3 FDA reports)
IMPULSE-CONTROL DISORDER ( 3 FDA reports)
INAPPROPRIATE AFFECT ( 3 FDA reports)
INCREASED APPETITE ( 3 FDA reports)
INFECTION ( 3 FDA reports)
INJECTION SITE DISCOLOURATION ( 3 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 3 FDA reports)
INTERVERTEBRAL DISCITIS ( 3 FDA reports)
INTRACRANIAL ANEURYSM ( 3 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
KERATITIS ( 3 FDA reports)
KNEE ARTHROPLASTY ( 3 FDA reports)
LACTOSE INTOLERANCE ( 3 FDA reports)
LIMB DISCOMFORT ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 3 FDA reports)
LYME DISEASE ( 3 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 3 FDA reports)
LYMPHOPENIA ( 3 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 3 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 3 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 3 FDA reports)
MESANGIOPROLIFERATIVE GLOMERULONEPHRITIS ( 3 FDA reports)
METASTASES TO LIVER ( 3 FDA reports)
MICROALBUMINURIA ( 3 FDA reports)
MICTURITION URGENCY ( 3 FDA reports)
MUSCLE FIBROSIS ( 3 FDA reports)
MUSCLE STRAIN ( 3 FDA reports)
MUSCLE TWITCHING ( 3 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 3 FDA reports)
MUSCULOSKELETAL PAIN ( 3 FDA reports)
MYOCARDITIS ( 3 FDA reports)
NEPHRITIS INTERSTITIAL ( 3 FDA reports)
NEPHROTIC SYNDROME ( 3 FDA reports)
NERVE INJURY ( 3 FDA reports)
NEURALGIA ( 3 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 3 FDA reports)
NEUROLOGICAL SYMPTOM ( 3 FDA reports)
NEUROTOXICITY ( 3 FDA reports)
OCULAR DISCOMFORT ( 3 FDA reports)
OEDEMA MOUTH ( 3 FDA reports)
OEDEMA MUCOSAL ( 3 FDA reports)
OSTEONECROSIS ( 3 FDA reports)
OSTEOPOROSIS ( 3 FDA reports)
PANCREATITIS ACUTE ( 3 FDA reports)
PARKINSON'S DISEASE ( 3 FDA reports)
PELVIC FLOOR MUSCLE WEAKNESS ( 3 FDA reports)
PERIPHERAL COLDNESS ( 3 FDA reports)
PERITONEAL DISORDER ( 3 FDA reports)
PERSONALITY CHANGE ( 3 FDA reports)
PHYSICAL ASSAULT ( 3 FDA reports)
PREMENSTRUAL SYNDROME ( 3 FDA reports)
PROCEDURAL SITE REACTION ( 3 FDA reports)
PROTHROMBIN TIME PROLONGED ( 3 FDA reports)
PSEUDOMONAS INFECTION ( 3 FDA reports)
PSEUDOPORPHYRIA ( 3 FDA reports)
QRS AXIS ABNORMAL ( 3 FDA reports)
QUADRIPLEGIA ( 3 FDA reports)
RADIUS FRACTURE ( 3 FDA reports)
RECTAL CANCER METASTATIC ( 3 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 3 FDA reports)
REHABILITATION THERAPY ( 3 FDA reports)
RENAL COLIC ( 3 FDA reports)
RENAL PAIN ( 3 FDA reports)
RENAL TUBERCULOSIS ( 3 FDA reports)
RESPIRATORY GAS EXCHANGE DISORDER ( 3 FDA reports)
RETROPERITONEAL FIBROSIS ( 3 FDA reports)
RHABDOMYOLYSIS ( 3 FDA reports)
SARCOIDOSIS ( 3 FDA reports)
SEROMA ( 3 FDA reports)
SINUS CONGESTION ( 3 FDA reports)
SOMNAMBULISM ( 3 FDA reports)
SPINAL OPERATION ( 3 FDA reports)
STAG HORN CALCULUS ( 3 FDA reports)
STOMACH DISCOMFORT ( 3 FDA reports)
STOMATITIS ( 3 FDA reports)
TACHYPNOEA ( 3 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 3 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 3 FDA reports)
THERAPY CESSATION ( 3 FDA reports)
THIRST ( 3 FDA reports)
TOBACCO USER ( 3 FDA reports)
TOOTH FRACTURE ( 3 FDA reports)
TOOTH INFECTION ( 3 FDA reports)
TRANSPLANT REJECTION ( 3 FDA reports)
URINE OUTPUT DECREASED ( 3 FDA reports)
UVEITIS ( 3 FDA reports)
VAGINAL INFECTION ( 3 FDA reports)
VICTIM OF HOMICIDE ( 3 FDA reports)
WEIGHT FLUCTUATION ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
WRIST FRACTURE ( 3 FDA reports)
ABSCESS ( 2 FDA reports)
ADRENAL INSUFFICIENCY ( 2 FDA reports)
ALCOHOL POISONING ( 2 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 2 FDA reports)
AMMONIA INCREASED ( 2 FDA reports)
ANGIONEUROTIC OEDEMA ( 2 FDA reports)
ANORGASMIA ( 2 FDA reports)
ANTIDEPRESSANT DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
ANTISOCIAL BEHAVIOUR ( 2 FDA reports)
ANTIVIRAL PROPHYLAXIS ( 2 FDA reports)
ANURIA ( 2 FDA reports)
AORTIC VALVE INCOMPETENCE ( 2 FDA reports)
APNOEA ( 2 FDA reports)
APPLICATION SITE IRRITATION ( 2 FDA reports)
APPLICATION SITE PRURITUS ( 2 FDA reports)
ARTERIAL STENT INSERTION ( 2 FDA reports)
ARTERIOGRAM CORONARY ( 2 FDA reports)
ARTERITIS ( 2 FDA reports)
ARTHROPOD BITE ( 2 FDA reports)
ASPIRATION ( 2 FDA reports)
ASPIRATION BRONCHIAL ( 2 FDA reports)
ASTIGMATISM ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 2 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 2 FDA reports)
AUTOIMMUNE THYROIDITIS ( 2 FDA reports)
BACTERIA URINE IDENTIFIED ( 2 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 2 FDA reports)
BILIARY DYSKINESIA ( 2 FDA reports)
BLADDER CANCER ( 2 FDA reports)
BLOOD BICARBONATE DECREASED ( 2 FDA reports)
BLOOD CHLORIDE DECREASED ( 2 FDA reports)
BLOOD CREATINE ( 2 FDA reports)
BLOOD CREATINE INCREASED ( 2 FDA reports)
BLOOD DISORDER ( 2 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 2 FDA reports)
BLOOD IRON DECREASED ( 2 FDA reports)
BRAIN HYPOXIA ( 2 FDA reports)
BRAIN INJURY ( 2 FDA reports)
BRAIN NEOPLASM ( 2 FDA reports)
BRUXISM ( 2 FDA reports)
BUTTOCK PAIN ( 2 FDA reports)
CARDIAC FAILURE CHRONIC ( 2 FDA reports)
CARDIAC FIBRILLATION ( 2 FDA reports)
CATARACT OPERATION ( 2 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 2 FDA reports)
CEREBROVASCULAR INSUFFICIENCY ( 2 FDA reports)
CERVICAL DYSPLASIA ( 2 FDA reports)
CHOLECYSTITIS CHRONIC ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
CHORIORETINOPATHY ( 2 FDA reports)
CHROMATURIA ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
COLITIS COLLAGENOUS ( 2 FDA reports)
COLITIS ULCERATIVE ( 2 FDA reports)
COLONIC POLYP ( 2 FDA reports)
COLOUR BLINDNESS ACQUIRED ( 2 FDA reports)
CONCUSSION ( 2 FDA reports)
CORONARY ARTERY STENOSIS ( 2 FDA reports)
DEAFNESS BILATERAL ( 2 FDA reports)
DEMYELINATION ( 2 FDA reports)
DERMATITIS ALLERGIC ( 2 FDA reports)
DERMATITIS BULLOUS ( 2 FDA reports)
DERMATITIS EXFOLIATIVE ( 2 FDA reports)
DEVICE FAILURE ( 2 FDA reports)
DIABETIC NEPHROPATHY ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DISSOCIATIVE DISORDER ( 2 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 2 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 2 FDA reports)
DRUG CLEARANCE DECREASED ( 2 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
EAR CONGESTION ( 2 FDA reports)
EAR INFECTION ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 2 FDA reports)
EMOTIONAL POVERTY ( 2 FDA reports)
ENTEROBACTER INFECTION ( 2 FDA reports)
EROSIVE OESOPHAGITIS ( 2 FDA reports)
ERUCTATION ( 2 FDA reports)
EXOSTOSIS ( 2 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 2 FDA reports)
EYE PRURITUS ( 2 FDA reports)
EYELID PAIN ( 2 FDA reports)
FACE INJURY ( 2 FDA reports)
FAECAL INCONTINENCE ( 2 FDA reports)
FEMALE GENITAL-DIGESTIVE TRACT FISTULA ( 2 FDA reports)
FEMORAL NECK FRACTURE ( 2 FDA reports)
FEMUR FRACTURE ( 2 FDA reports)
FLUID INTAKE REDUCED ( 2 FDA reports)
FOOD CRAVING ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 2 FDA reports)
GASTROINTESTINAL NECROSIS ( 2 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
GINGIVAL BLEEDING ( 2 FDA reports)
GINGIVAL ERYTHEMA ( 2 FDA reports)
GINGIVAL OPERATION ( 2 FDA reports)
GLOSSODYNIA ( 2 FDA reports)
GOUT ( 2 FDA reports)
GYNAECOMASTIA ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HAEMOGLOBIN INCREASED ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 2 FDA reports)
HAIR GROWTH ABNORMAL ( 2 FDA reports)
HAND FRACTURE ( 2 FDA reports)
HEART SOUNDS ABNORMAL ( 2 FDA reports)
HELICOBACTER GASTRITIS ( 2 FDA reports)
HEMIANOPIA HOMONYMOUS ( 2 FDA reports)
HEPATIC ADENOMA ( 2 FDA reports)
HEPATIC ENZYME ABNORMAL ( 2 FDA reports)
HEPATIC NECROSIS ( 2 FDA reports)
HEPATIC NEOPLASM ( 2 FDA reports)
HEPATITIS C ( 2 FDA reports)
HERPES VIRUS INFECTION ( 2 FDA reports)
HIATUS HERNIA ( 2 FDA reports)
HOMICIDE ( 2 FDA reports)
HUMERUS FRACTURE ( 2 FDA reports)
HYPERCOAGULATION ( 2 FDA reports)
HYPERLIPIDAEMIA ( 2 FDA reports)
HYPERMETROPIA ( 2 FDA reports)
HYPERPHOSPHATAEMIA ( 2 FDA reports)
HYPERTONIA ( 2 FDA reports)
HYPOAESTHESIA FACIAL ( 2 FDA reports)
HYPOGLYCAEMIC ENCEPHALOPATHY ( 2 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 2 FDA reports)
HYPOTONIA ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 2 FDA reports)
IMMOBILE ( 2 FDA reports)
INCISIONAL HERNIA ( 2 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 2 FDA reports)
INFECTIOUS PERITONITIS ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
INJECTION SITE DISCOMFORT ( 2 FDA reports)
INJECTION SITE MASS ( 2 FDA reports)
INJECTION SITE RASH ( 2 FDA reports)
INJURY CORNEAL ( 2 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 2 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE EXPELLED ( 2 FDA reports)
IUD MIGRATION ( 2 FDA reports)
JOINT ARTHROPLASTY ( 2 FDA reports)
JOINT SPRAIN ( 2 FDA reports)
KIDNEY INFECTION ( 2 FDA reports)
KLEBSIELLA INFECTION ( 2 FDA reports)
LACERATION ( 2 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LEUKOENCEPHALOPATHY ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LIGAMENT SPRAIN ( 2 FDA reports)
LIP DISORDER ( 2 FDA reports)
LIVER INJURY ( 2 FDA reports)
LOWER LIMB FRACTURE ( 2 FDA reports)
LUNG ABSCESS ( 2 FDA reports)
LYMPHOEDEMA ( 2 FDA reports)
MASTECTOMY ( 2 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
MEDICAL DEVICE REMOVAL ( 2 FDA reports)
MEDICATION RESIDUE ( 2 FDA reports)
MENORRHAGIA ( 2 FDA reports)
METABOLIC ENCEPHALOPATHY ( 2 FDA reports)
MIDDLE EAR EFFUSION ( 2 FDA reports)
MIOSIS ( 2 FDA reports)
MOUTH ULCERATION ( 2 FDA reports)
MULTIPLE ALLERGIES ( 2 FDA reports)
MULTIPLE MYELOMA ( 2 FDA reports)
MUSCLE CRAMP ( 2 FDA reports)
MUSCLE RIGIDITY ( 2 FDA reports)
MUSCLE TIGHTNESS ( 2 FDA reports)
MYCOSIS FUNGOIDES ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
NAIL BED BLEEDING ( 2 FDA reports)
NAIL DISORDER ( 2 FDA reports)
NEOPLASM ( 2 FDA reports)
NEPHROPATHY ( 2 FDA reports)
NEUROPATHY ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
NOCTURIA ( 2 FDA reports)
NYSTAGMUS ( 2 FDA reports)
OCULAR HYPERAEMIA ( 2 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 2 FDA reports)
OESOPHAGEAL CARCINOMA ( 2 FDA reports)
OESOPHAGITIS ( 2 FDA reports)
ONYCHOCLASIS ( 2 FDA reports)
OPEN WOUND ( 2 FDA reports)
OPTIC NEURITIS ( 2 FDA reports)
ORGANISING PNEUMONIA ( 2 FDA reports)
ORTHOPNOEA ( 2 FDA reports)
OSTEOMYELITIS FUNGAL ( 2 FDA reports)
OVARIAN CYST ( 2 FDA reports)
PAIN IN JAW ( 2 FDA reports)
PANCREATIC INSUFFICIENCY ( 2 FDA reports)
PANCREATITIS CHRONIC ( 2 FDA reports)
PARESIS ( 2 FDA reports)
PCO2 DECREASED ( 2 FDA reports)
PELVIC MASS ( 2 FDA reports)
PELVIC PAIN ( 2 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 2 FDA reports)
PERITONEAL NEOPLASM ( 2 FDA reports)
PERITONITIS BACTERIAL ( 2 FDA reports)
PERTUSSIS ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
PINGUECULA ( 2 FDA reports)
PITUITARY TUMOUR ( 2 FDA reports)
PLATELET COUNT INCREASED ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
POLYNEUROPATHY ( 2 FDA reports)
POLYTRAUMATISM ( 2 FDA reports)
PRECANCEROUS CELLS PRESENT ( 2 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 2 FDA reports)
PREMATURE LABOUR ( 2 FDA reports)
PRIMARY SEQUESTRUM ( 2 FDA reports)
PRODUCT PHYSICAL ISSUE ( 2 FDA reports)
PROSTATE CANCER ( 2 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 2 FDA reports)
PULSE PRESSURE DECREASED ( 2 FDA reports)
RASH MACULAR ( 2 FDA reports)
RASH PAPULAR ( 2 FDA reports)
RASH PUSTULAR ( 2 FDA reports)
RECTAL ABSCESS ( 2 FDA reports)
RESPIRATORY RATE DECREASED ( 2 FDA reports)
RETICULIN INCREASED ( 2 FDA reports)
RHINORRHOEA ( 2 FDA reports)
RHONCHI ( 2 FDA reports)
RIGHT VENTRICULAR FAILURE ( 2 FDA reports)
SALIVARY HYPERSECRETION ( 2 FDA reports)
SCAR ( 2 FDA reports)
SCRATCH ( 2 FDA reports)
SEPTIC EMBOLUS ( 2 FDA reports)
SERUM FERRITIN INCREASED ( 2 FDA reports)
SJOGREN'S SYNDROME ( 2 FDA reports)
SKIN CHAPPED ( 2 FDA reports)
SLEEP TERROR ( 2 FDA reports)
SLEEP WALKING ( 2 FDA reports)
SLUGGISHNESS ( 2 FDA reports)
SMALL INTESTINE CARCINOMA ( 2 FDA reports)
SPINAL DISORDER ( 2 FDA reports)
SPUTUM DISCOLOURED ( 2 FDA reports)
SUBDURAL HAEMATOMA ( 2 FDA reports)
SUFFOCATION FEELING ( 2 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 2 FDA reports)
TACHYPHYLAXIS ( 2 FDA reports)
TENDERNESS ( 2 FDA reports)
TENDON RUPTURE ( 2 FDA reports)
TENSION HEADACHE ( 2 FDA reports)
THERMAL BURN ( 2 FDA reports)
THROMBOPHLEBITIS ( 2 FDA reports)
TONGUE OEDEMA ( 2 FDA reports)
TOOTH DISORDER ( 2 FDA reports)
TRACHEOSTOMY ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
TRIGGER FINGER ( 2 FDA reports)
TROPONIN INCREASED ( 2 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 2 FDA reports)
UNINTENDED PREGNANCY ( 2 FDA reports)
UPPER LIMB FRACTURE ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
URINE ABNORMALITY ( 2 FDA reports)
UTERINE ENLARGEMENT ( 2 FDA reports)
VAGINAL DISCHARGE ( 2 FDA reports)
VARICOSE VEIN ( 2 FDA reports)
VENOUS THROMBOSIS LIMB ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
VERBAL ABUSE ( 2 FDA reports)
VICTIM OF SEXUAL ABUSE ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
VISUAL FIELD DEFECT ( 2 FDA reports)
WHIPLASH INJURY ( 2 FDA reports)
ABDOMINAL ABSCESS ( 1 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ABORTION SPONTANEOUS COMPLETE ( 1 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 1 FDA reports)
ACCIDENTAL NEEDLE STICK ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACUTE MONOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ADVERSE REACTION ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
ALCOHOL ABUSE ( 1 FDA reports)
ALCOHOL INTERACTION ( 1 FDA reports)
ALCOHOL INTOLERANCE ( 1 FDA reports)
ALLODYNIA ( 1 FDA reports)
AMPHETAMINES POSITIVE ( 1 FDA reports)
ANALGESIC THERAPY ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANASTOMOTIC COMPLICATION ( 1 FDA reports)
ANGIOGRAM ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
ANIMAL BITE ( 1 FDA reports)
ANION GAP INCREASED ( 1 FDA reports)
ANTIDEPRESSANT THERAPY ( 1 FDA reports)
ANXIETY DISORDER ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
APHONIA ( 1 FDA reports)
APPENDICEAL ABSCESS ( 1 FDA reports)
APPENDICITIS PERFORATED ( 1 FDA reports)
APPENDIX DISORDER ( 1 FDA reports)
APPLICATION SITE BURN ( 1 FDA reports)
APPLICATION SITE EXCORIATION ( 1 FDA reports)
APPLICATION SITE PAIN ( 1 FDA reports)
APPLICATION SITE PHOTOSENSITIVITY REACTION ( 1 FDA reports)
APPLICATION SITE URTICARIA ( 1 FDA reports)
APPLICATION SITE VESICLES ( 1 FDA reports)
APTYALISM ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 1 FDA reports)
ARTERIAL DISORDER ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ASTERIXIS ( 1 FDA reports)
ATRIAL THROMBOSIS ( 1 FDA reports)
AURICULAR SWELLING ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BACTERIAL TEST POSITIVE ( 1 FDA reports)
BACTERIURIA ( 1 FDA reports)
BALANOPOSTHITIS ( 1 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
BEHCET'S SYNDROME ( 1 FDA reports)
BENIGN NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BINGE EATING ( 1 FDA reports)
BLADDER DISTENSION ( 1 FDA reports)
BLADDER NECK OBSTRUCTION ( 1 FDA reports)
BLADDER REPAIR ( 1 FDA reports)
BLEEDING TIME PROLONGED ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN DECREASED ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 1 FDA reports)
BLOOD IRON INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BODY FAT DISORDER ( 1 FDA reports)
BONE CYST ( 1 FDA reports)
BONE MARROW TRANSPLANT ( 1 FDA reports)
BONE NEOPLASM MALIGNANT ( 1 FDA reports)
BONE OPERATION ( 1 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 1 FDA reports)
BRADYARRHYTHMIA ( 1 FDA reports)
BRAIN DAMAGE ( 1 FDA reports)
BRAIN MIDLINE SHIFT ( 1 FDA reports)
BRAIN NEOPLASM BENIGN ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BREAST CANCER STAGE I ( 1 FDA reports)
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BREAST PAIN ( 1 FDA reports)
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BREATH ODOUR ( 1 FDA reports)
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BRONCHIAL NEOPLASM ( 1 FDA reports)
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BRONCHOSPASM ( 1 FDA reports)
BULIMIA NERVOSA ( 1 FDA reports)
BUNDLE BRANCH BLOCK ( 1 FDA reports)
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BURNOUT SYNDROME ( 1 FDA reports)
BURSITIS ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CAPSULE PHYSICAL ISSUE ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
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CARDIAC VALVE DISEASE ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIO-RESPIRATORY DISTRESS ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CARDIOTHORACIC RATIO INCREASED ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 1 FDA reports)
CARDITIS ( 1 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 1 FDA reports)
CAROTID ARTERY DISEASE ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
CAVERNOUS SINUS THROMBOSIS ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
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CEREBELLAR ATROPHY ( 1 FDA reports)
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CEREBRAL ARTERY EMBOLISM ( 1 FDA reports)
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CHANGE OF BOWEL HABIT ( 1 FDA reports)
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CHOLECYSTECTOMY ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOREA ( 1 FDA reports)
CHRONIC HEPATITIS ( 1 FDA reports)
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CONGENITAL CHOROID PLEXUS CYST ( 1 FDA reports)
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CONGENITAL VISUAL ACUITY REDUCED ( 1 FDA reports)
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CONVULSIVE THRESHOLD LOWERED ( 1 FDA reports)
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CULTURE POSITIVE ( 1 FDA reports)
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CYST ( 1 FDA reports)
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DIABETIC EYE DISEASE ( 1 FDA reports)
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DISLOCATION OF VERTEBRA ( 1 FDA reports)
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DIZZINESS POSTURAL ( 1 FDA reports)
DRESSLER'S SYNDROME ( 1 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG REHABILITATION ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
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DRUG WITHDRAWAL HEADACHE ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 1 FDA reports)
DUODENAL STENOSIS ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
EAR DISORDER ( 1 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
ECTOPIC PREGNANCY ( 1 FDA reports)
EDUCATIONAL PROBLEM ( 1 FDA reports)
ELECTRIC SHOCK ( 1 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
ELECTROCONVULSIVE THERAPY ( 1 FDA reports)
EMBOLIC STROKE ( 1 FDA reports)
ENCEPHALOMALACIA ( 1 FDA reports)
ENDOSCOPY ( 1 FDA reports)
ENTEROCOCCAL SEPSIS ( 1 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 1 FDA reports)
ENTEROCUTANEOUS FISTULA ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
EXPOSED BONE IN JAW ( 1 FDA reports)
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EYE DISCHARGE ( 1 FDA reports)
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EYE INJURY ( 1 FDA reports)
EYE LASER SURGERY ( 1 FDA reports)
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FACTOR V LEIDEN MUTATION ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
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FEELING DRUNK ( 1 FDA reports)
FEELING HOT AND COLD ( 1 FDA reports)
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FLUID OVERLOAD ( 1 FDA reports)
FOETAL EXPOSURE TIMING UNSPECIFIED ( 1 FDA reports)
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FRUSTRATION ( 1 FDA reports)
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GASTRIC BYPASS ( 1 FDA reports)
GASTRIC DILATATION ( 1 FDA reports)
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GASTRIC VARICES ( 1 FDA reports)
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HAEMODYNAMIC REBOUND ( 1 FDA reports)
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HAEMORRHOIDS ( 1 FDA reports)
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HEPATITIS ACUTE ( 1 FDA reports)
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ILLUSION ( 1 FDA reports)
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INJECTION SITE BRUISING ( 1 FDA reports)
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LABELLED DRUG-DRUG INTERACTION MEDICATION ERROR ( 1 FDA reports)
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MASKED FACIES ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
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PACEMAKER GENERATED RHYTHM ( 1 FDA reports)
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