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

PAIN ( 178 FDA reports)
ANXIETY ( 147 FDA reports)
FATIGUE ( 119 FDA reports)
DEPRESSION ( 113 FDA reports)
HEADACHE ( 103 FDA reports)
NAUSEA ( 92 FDA reports)
DRUG INEFFECTIVE ( 90 FDA reports)
INJURY ( 85 FDA reports)
EMOTIONAL DISTRESS ( 69 FDA reports)
FALL ( 69 FDA reports)
WEIGHT INCREASED ( 66 FDA reports)
DIZZINESS ( 65 FDA reports)
VOMITING ( 65 FDA reports)
INSOMNIA ( 64 FDA reports)
PULMONARY EMBOLISM ( 60 FDA reports)
CHEST PAIN ( 59 FDA reports)
DYSPNOEA ( 57 FDA reports)
SOMNOLENCE ( 56 FDA reports)
DEEP VEIN THROMBOSIS ( 52 FDA reports)
MALAISE ( 52 FDA reports)
ASTHENIA ( 51 FDA reports)
BACK PAIN ( 50 FDA reports)
DIARRHOEA ( 50 FDA reports)
FEELING ABNORMAL ( 47 FDA reports)
ABDOMINAL PAIN UPPER ( 45 FDA reports)
CHOLECYSTITIS CHRONIC ( 45 FDA reports)
RASH ( 45 FDA reports)
NECK PAIN ( 40 FDA reports)
ABDOMINAL PAIN ( 37 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 37 FDA reports)
OEDEMA PERIPHERAL ( 37 FDA reports)
ANHEDONIA ( 36 FDA reports)
PAIN IN EXTREMITY ( 36 FDA reports)
SINUSITIS ( 36 FDA reports)
SUICIDAL IDEATION ( 36 FDA reports)
TREMOR ( 35 FDA reports)
DRUG EFFECT DECREASED ( 34 FDA reports)
GALLBLADDER DISORDER ( 34 FDA reports)
ARTHRALGIA ( 33 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 33 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 32 FDA reports)
HYPERHIDROSIS ( 32 FDA reports)
MUSCULAR WEAKNESS ( 32 FDA reports)
MENTAL DISORDER ( 31 FDA reports)
AGGRESSION ( 30 FDA reports)
CONFUSIONAL STATE ( 30 FDA reports)
CONVULSION ( 30 FDA reports)
DYSPEPSIA ( 30 FDA reports)
PNEUMONIA ( 30 FDA reports)
ABDOMINAL DISCOMFORT ( 29 FDA reports)
VISUAL IMPAIRMENT ( 29 FDA reports)
HYPOAESTHESIA ( 28 FDA reports)
BLOOD PRESSURE INCREASED ( 27 FDA reports)
DRUG DOSE OMISSION ( 27 FDA reports)
GASTRITIS ( 27 FDA reports)
MEMORY IMPAIRMENT ( 27 FDA reports)
VISION BLURRED ( 27 FDA reports)
ABNORMAL BEHAVIOUR ( 26 FDA reports)
AMNESIA ( 26 FDA reports)
DYSPHAGIA ( 26 FDA reports)
PRURITUS ( 26 FDA reports)
MENTAL STATUS CHANGES ( 25 FDA reports)
MOOD SWINGS ( 25 FDA reports)
MUSCLE SPASMS ( 25 FDA reports)
ABDOMINAL DISTENSION ( 24 FDA reports)
CONSTIPATION ( 24 FDA reports)
CONTUSION ( 24 FDA reports)
DYSKINESIA ( 24 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 23 FDA reports)
OSTEOPENIA ( 23 FDA reports)
PYREXIA ( 23 FDA reports)
ANAEMIA ( 22 FDA reports)
ANGER ( 22 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 22 FDA reports)
CERVICAL SPINAL STENOSIS ( 22 FDA reports)
DEHYDRATION ( 22 FDA reports)
LOSS OF CONSCIOUSNESS ( 22 FDA reports)
MENSTRUATION IRREGULAR ( 22 FDA reports)
MIGRAINE ( 22 FDA reports)
OSTEOARTHRITIS ( 22 FDA reports)
OSTEONECROSIS OF JAW ( 22 FDA reports)
SPINAL OSTEOARTHRITIS ( 22 FDA reports)
AGITATION ( 21 FDA reports)
ATELECTASIS ( 21 FDA reports)
BIPOLAR DISORDER ( 21 FDA reports)
CHOLELITHIASIS ( 21 FDA reports)
COGNITIVE DISORDER ( 21 FDA reports)
INJECTION SITE PAIN ( 21 FDA reports)
RECTAL POLYP ( 21 FDA reports)
EAR PAIN ( 20 FDA reports)
MYALGIA ( 20 FDA reports)
SYNOVIAL CYST ( 20 FDA reports)
WEIGHT DECREASED ( 20 FDA reports)
HYPERLIPIDAEMIA ( 19 FDA reports)
URINARY TRACT INFECTION ( 19 FDA reports)
VIRAL INFECTION ( 19 FDA reports)
HAEMATOCHEZIA ( 18 FDA reports)
NEOPLASM MALIGNANT ( 18 FDA reports)
NIGHTMARE ( 18 FDA reports)
OESOPHAGITIS ( 18 FDA reports)
OFF LABEL USE ( 18 FDA reports)
PALPITATIONS ( 18 FDA reports)
PLEURAL FIBROSIS ( 18 FDA reports)
ARTHROPATHY ( 17 FDA reports)
BLOOD PRESSURE DECREASED ( 17 FDA reports)
EMOTIONAL DISORDER ( 17 FDA reports)
GAIT DISTURBANCE ( 17 FDA reports)
HEPATITIS ( 17 FDA reports)
MANIA ( 17 FDA reports)
NASAL CONGESTION ( 17 FDA reports)
NERVOUSNESS ( 17 FDA reports)
PARAESTHESIA ( 17 FDA reports)
RECTAL HAEMORRHAGE ( 17 FDA reports)
SUICIDE ATTEMPT ( 17 FDA reports)
CEREBROVASCULAR ACCIDENT ( 16 FDA reports)
COUGH ( 16 FDA reports)
DIVERTICULUM ( 16 FDA reports)
DRY MOUTH ( 16 FDA reports)
FIBROMYALGIA ( 16 FDA reports)
FLUID RETENTION ( 16 FDA reports)
HAEMORRHOIDS ( 16 FDA reports)
HALLUCINATION ( 16 FDA reports)
INCORRECT DOSE ADMINISTERED ( 16 FDA reports)
MULTIPLE SCLEROSIS ( 16 FDA reports)
MUSCULOSKELETAL PAIN ( 16 FDA reports)
SUBSTANCE ABUSE ( 16 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 16 FDA reports)
ACNE ( 15 FDA reports)
ADNEXA UTERI MASS ( 15 FDA reports)
ARTERIOSCLEROSIS ( 15 FDA reports)
BONE LESION ( 15 FDA reports)
DENTAL CARIES ( 15 FDA reports)
DYSAESTHESIA ( 15 FDA reports)
FRACTURED SACRUM ( 15 FDA reports)
GASTRIC POLYPS ( 15 FDA reports)
HEPATIC CYST ( 15 FDA reports)
HEPATIC LESION ( 15 FDA reports)
HEPATIC MASS ( 15 FDA reports)
HIATUS HERNIA ( 15 FDA reports)
HYPERCHOLESTEROLAEMIA ( 15 FDA reports)
LETHARGY ( 15 FDA reports)
LYMPHOEDEMA ( 15 FDA reports)
NASAL SEPTUM DEVIATION ( 15 FDA reports)
NEOPLASM PROGRESSION ( 15 FDA reports)
OSTEOCHONDROSIS ( 15 FDA reports)
PANCREATITIS ( 15 FDA reports)
SCOLIOSIS ( 15 FDA reports)
SPLENIC LESION ( 15 FDA reports)
SPONDYLOLISTHESIS ( 15 FDA reports)
SPONDYLOLYSIS ( 15 FDA reports)
TONGUE DISCOLOURATION ( 15 FDA reports)
VAGINAL DISCHARGE ( 15 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 15 FDA reports)
BENIGN OVARIAN TUMOUR ( 14 FDA reports)
BONE PAIN ( 14 FDA reports)
DEPRESSED MOOD ( 14 FDA reports)
DISORIENTATION ( 14 FDA reports)
DRUG INTERACTION ( 14 FDA reports)
FEAR ( 14 FDA reports)
IMPAIRED DRIVING ABILITY ( 14 FDA reports)
INTENTIONAL DRUG MISUSE ( 14 FDA reports)
OSTEOPOROSIS ( 14 FDA reports)
STRESS ( 14 FDA reports)
TINNITUS ( 14 FDA reports)
WITHDRAWAL SYNDROME ( 14 FDA reports)
BALANCE DISORDER ( 13 FDA reports)
CRYING ( 13 FDA reports)
GALLBLADDER INJURY ( 13 FDA reports)
IRRITABILITY ( 13 FDA reports)
KERATITIS ( 13 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 13 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 13 FDA reports)
RENAL FAILURE CHRONIC ( 13 FDA reports)
RESPIRATORY FAILURE ( 13 FDA reports)
SENSITIVITY OF TEETH ( 13 FDA reports)
VERTIGO ( 13 FDA reports)
CHILLS ( 12 FDA reports)
DECREASED APPETITE ( 12 FDA reports)
JOINT SWELLING ( 12 FDA reports)
LACERATION ( 12 FDA reports)
NASOPHARYNGITIS ( 12 FDA reports)
NEUROPATHY PERIPHERAL ( 12 FDA reports)
OVERDOSE ( 12 FDA reports)
SPEECH DISORDER ( 12 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 12 FDA reports)
URTICARIA ( 12 FDA reports)
ACTINIC KERATOSIS ( 11 FDA reports)
BILIARY DYSKINESIA ( 11 FDA reports)
CHOLESTEATOMA ( 11 FDA reports)
CONDITION AGGRAVATED ( 11 FDA reports)
COORDINATION ABNORMAL ( 11 FDA reports)
DEAFNESS NEUROSENSORY ( 11 FDA reports)
DERMATITIS ( 11 FDA reports)
DISTURBANCE IN ATTENTION ( 11 FDA reports)
DRUG DEPENDENCE ( 11 FDA reports)
DYSTONIA ( 11 FDA reports)
ERYTHEMA ( 11 FDA reports)
GASTROINTESTINAL DISORDER ( 11 FDA reports)
HEART RATE INCREASED ( 11 FDA reports)
INFECTION ( 11 FDA reports)
INFLUENZA LIKE ILLNESS ( 11 FDA reports)
MENTAL IMPAIRMENT ( 11 FDA reports)
NEURITIS ( 11 FDA reports)
NEURODERMATITIS ( 11 FDA reports)
PAPILLOMA ( 11 FDA reports)
PARANOIA ( 11 FDA reports)
PARONYCHIA ( 11 FDA reports)
PHLEBITIS ( 11 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 11 FDA reports)
ROAD TRAFFIC ACCIDENT ( 11 FDA reports)
SWOLLEN TONGUE ( 11 FDA reports)
TARDIVE DYSKINESIA ( 11 FDA reports)
THINKING ABNORMAL ( 11 FDA reports)
VULVOVAGINITIS ( 11 FDA reports)
ANIMAL BITE ( 10 FDA reports)
CACHEXIA ( 10 FDA reports)
CATATONIA ( 10 FDA reports)
DEATH ( 10 FDA reports)
DYSARTHRIA ( 10 FDA reports)
HAEMATEMESIS ( 10 FDA reports)
HYPERSENSITIVITY ( 10 FDA reports)
INTENTIONAL OVERDOSE ( 10 FDA reports)
MASS ( 10 FDA reports)
PANIC ATTACK ( 10 FDA reports)
PRODUCT QUALITY ISSUE ( 10 FDA reports)
PSYCHOTIC DISORDER ( 10 FDA reports)
RENAL FAILURE ( 10 FDA reports)
RENAL FAILURE ACUTE ( 10 FDA reports)
TYPE 2 DIABETES MELLITUS ( 10 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 9 FDA reports)
BRAIN INJURY ( 9 FDA reports)
CARDIOMEGALY ( 9 FDA reports)
CHEST DISCOMFORT ( 9 FDA reports)
CHOLECYSTITIS ( 9 FDA reports)
DIABETES MELLITUS ( 9 FDA reports)
DYSGEUSIA ( 9 FDA reports)
EATING DISORDER ( 9 FDA reports)
FLUSHING ( 9 FDA reports)
HEAD INJURY ( 9 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 9 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 9 FDA reports)
MULTIPLE DRUG OVERDOSE ( 9 FDA reports)
PANIC DISORDER ( 9 FDA reports)
PSYCHOLOGICAL TRAUMA ( 9 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 9 FDA reports)
SWELLING ( 9 FDA reports)
SYNCOPE ( 9 FDA reports)
THROMBOSIS ( 9 FDA reports)
ABNORMAL DREAMS ( 8 FDA reports)
ADVERSE EVENT ( 8 FDA reports)
ALOPECIA ( 8 FDA reports)
ARTHRITIS ( 8 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 8 FDA reports)
BREAST CANCER ( 8 FDA reports)
CHOLECYSTECTOMY ( 8 FDA reports)
CHOLECYSTITIS ACUTE ( 8 FDA reports)
COLONIC POLYP ( 8 FDA reports)
CYST ( 8 FDA reports)
DIVERTICULUM INTESTINAL ( 8 FDA reports)
DRUG ABUSE ( 8 FDA reports)
DYSPNOEA EXERTIONAL ( 8 FDA reports)
DYSURIA ( 8 FDA reports)
ERECTILE DYSFUNCTION ( 8 FDA reports)
EUPHORIC MOOD ( 8 FDA reports)
FEELING OF DESPAIR ( 8 FDA reports)
GRAND MAL CONVULSION ( 8 FDA reports)
HOSTILITY ( 8 FDA reports)
HOT FLUSH ( 8 FDA reports)
HYPOKALAEMIA ( 8 FDA reports)
INJECTION SITE ERYTHEMA ( 8 FDA reports)
INJECTION SITE HAEMATOMA ( 8 FDA reports)
PNEUMOTHORAX ( 8 FDA reports)
POLLAKIURIA ( 8 FDA reports)
RESPIRATORY ARREST ( 8 FDA reports)
RHEUMATOID ARTHRITIS ( 8 FDA reports)
ROTATOR CUFF SYNDROME ( 8 FDA reports)
VISUAL ACUITY REDUCED ( 8 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 7 FDA reports)
BRONCHITIS ( 7 FDA reports)
CARDIAC DISORDER ( 7 FDA reports)
CEREBROVASCULAR DISORDER ( 7 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 7 FDA reports)
COLITIS ULCERATIVE ( 7 FDA reports)
CYANOSIS ( 7 FDA reports)
DEVICE MALFUNCTION ( 7 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 7 FDA reports)
DYSPHONIA ( 7 FDA reports)
EMPYEMA ( 7 FDA reports)
FOOT FRACTURE ( 7 FDA reports)
GLOSSODYNIA ( 7 FDA reports)
HEPATIC ENZYME INCREASED ( 7 FDA reports)
HYPOTENSION ( 7 FDA reports)
IMPAIRED REASONING ( 7 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 7 FDA reports)
MASTICATION DISORDER ( 7 FDA reports)
MEDICATION ERROR ( 7 FDA reports)
MUSCLE ATROPHY ( 7 FDA reports)
MUSCLE SPASTICITY ( 7 FDA reports)
MUSCLE TWITCHING ( 7 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 7 FDA reports)
OROPHARYNGEAL PAIN ( 7 FDA reports)
PERONEAL NERVE PALSY ( 7 FDA reports)
RETCHING ( 7 FDA reports)
RHINITIS ( 7 FDA reports)
RIB FRACTURE ( 7 FDA reports)
SHOCK ( 7 FDA reports)
SWELLING FACE ( 7 FDA reports)
TENDERNESS ( 7 FDA reports)
TIBIA FRACTURE ( 7 FDA reports)
TOOTH FRACTURE ( 7 FDA reports)
TOOTHACHE ( 7 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 7 FDA reports)
ABSCESS ( 6 FDA reports)
ALLODYNIA ( 6 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST ( 6 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 6 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
BACTERIAL DISEASE CARRIER ( 6 FDA reports)
BLADDER DISCOMFORT ( 6 FDA reports)
BLINDNESS ( 6 FDA reports)
BLISTER ( 6 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 6 FDA reports)
BRONCHOPLEURAL FISTULA ( 6 FDA reports)
BURNING SENSATION ( 6 FDA reports)
CANCER PAIN ( 6 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 6 FDA reports)
CHOLECYSTITIS INFECTIVE ( 6 FDA reports)
CHONDROMALACIA ( 6 FDA reports)
DECREASED INTEREST ( 6 FDA reports)
DEPRESSION SUICIDAL ( 6 FDA reports)
DIPLOPIA ( 6 FDA reports)
DRUG ADMINISTRATION ERROR ( 6 FDA reports)
DRUG INTOLERANCE ( 6 FDA reports)
EAR INFECTION ( 6 FDA reports)
EMPHYSEMA ( 6 FDA reports)
EYE DISCHARGE ( 6 FDA reports)
FAECAL INCONTINENCE ( 6 FDA reports)
FIBULA FRACTURE ( 6 FDA reports)
FOOT DEFORMITY ( 6 FDA reports)
HYDROPNEUMOTHORAX ( 6 FDA reports)
HYPERAESTHESIA ( 6 FDA reports)
HYPERTENSION ( 6 FDA reports)
ILL-DEFINED DISORDER ( 6 FDA reports)
INJURY CORNEAL ( 6 FDA reports)
INTERCOSTAL NEURALGIA ( 6 FDA reports)
IRRITABLE BOWEL SYNDROME ( 6 FDA reports)
LIP DISCOLOURATION ( 6 FDA reports)
LUNG INFECTION ( 6 FDA reports)
LUNG NEOPLASM MALIGNANT ( 6 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 6 FDA reports)
MALIGNANT HYPERTENSION ( 6 FDA reports)
MENOPAUSE ( 6 FDA reports)
METASTASES TO LYMPH NODES ( 6 FDA reports)
OBESITY ( 6 FDA reports)
ORAL PAIN ( 6 FDA reports)
OSTEORADIONECROSIS ( 6 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 6 FDA reports)
POLYURIA ( 6 FDA reports)
POTENTIATING DRUG INTERACTION ( 6 FDA reports)
PREGNANCY ( 6 FDA reports)
PULMONARY AIR LEAKAGE ( 6 FDA reports)
PULMONARY FIBROSIS ( 6 FDA reports)
RASH PRURITIC ( 6 FDA reports)
RESTLESSNESS ( 6 FDA reports)
RHABDOMYOLYSIS ( 6 FDA reports)
SCAR ( 6 FDA reports)
SENSORY DISTURBANCE ( 6 FDA reports)
SLEEP DISORDER ( 6 FDA reports)
TENDON RUPTURE ( 6 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 6 FDA reports)
THROAT TIGHTNESS ( 6 FDA reports)
THROMBOCYTOPENIA ( 6 FDA reports)
TOOTH DISORDER ( 6 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 6 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 6 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 6 FDA reports)
URINARY INCONTINENCE ( 6 FDA reports)
VAGINAL HAEMORRHAGE ( 6 FDA reports)
WHEEZING ( 6 FDA reports)
ACCIDENTAL OVERDOSE ( 5 FDA reports)
ADVERSE DRUG REACTION ( 5 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
ANKLE FRACTURE ( 5 FDA reports)
ASTHMA ( 5 FDA reports)
BACK DISORDER ( 5 FDA reports)
BLOOD CALCIUM DECREASED ( 5 FDA reports)
BREAST CALCIFICATIONS ( 5 FDA reports)
CARPAL TUNNEL SYNDROME ( 5 FDA reports)
CELLULITIS ( 5 FDA reports)
CROHN'S DISEASE ( 5 FDA reports)
DRUG DETOXIFICATION ( 5 FDA reports)
ELECTROLYTE IMBALANCE ( 5 FDA reports)
FEELING HOT ( 5 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 5 FDA reports)
HALLUCINATION, AUDITORY ( 5 FDA reports)
HALLUCINATION, VISUAL ( 5 FDA reports)
HYPERGLYCAEMIA ( 5 FDA reports)
HYPERVENTILATION ( 5 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 5 FDA reports)
INCREASED APPETITE ( 5 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 5 FDA reports)
INJECTION SITE REACTION ( 5 FDA reports)
INTESTINAL OBSTRUCTION ( 5 FDA reports)
KIDNEY INFECTION ( 5 FDA reports)
LOCALISED INFECTION ( 5 FDA reports)
MALIGNANT MELANOMA ( 5 FDA reports)
MYOCARDIAL INFARCTION ( 5 FDA reports)
NERVOUS SYSTEM DISORDER ( 5 FDA reports)
NO ADVERSE EVENT ( 5 FDA reports)
PHARYNGEAL DISORDER ( 5 FDA reports)
POOR QUALITY SLEEP ( 5 FDA reports)
PROCEDURAL PAIN ( 5 FDA reports)
SINUS BRADYCARDIA ( 5 FDA reports)
SPINAL COLUMN STENOSIS ( 5 FDA reports)
STAPHYLOCOCCAL INFECTION ( 5 FDA reports)
TACHYCARDIA ( 5 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 5 FDA reports)
TONGUE DISORDER ( 5 FDA reports)
ABORTION SPONTANEOUS ( 4 FDA reports)
AMENORRHOEA ( 4 FDA reports)
APHASIA ( 4 FDA reports)
BLOOD ALBUMIN DECREASED ( 4 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 4 FDA reports)
BLOOD POTASSIUM DECREASED ( 4 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 4 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 4 FDA reports)
BRAIN DEATH ( 4 FDA reports)
BRAIN OEDEMA ( 4 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 4 FDA reports)
COAGULOPATHY ( 4 FDA reports)
COMA ( 4 FDA reports)
DEMYELINATION ( 4 FDA reports)
DETOXIFICATION ( 4 FDA reports)
DIABETIC KETOACIDOSIS ( 4 FDA reports)
DRUG DIVERSION ( 4 FDA reports)
DRUG PRESCRIBING ERROR ( 4 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 4 FDA reports)
DRUG SCREEN POSITIVE ( 4 FDA reports)
DRY SKIN ( 4 FDA reports)
ECONOMIC PROBLEM ( 4 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 4 FDA reports)
EPILEPSY ( 4 FDA reports)
EXPOSED BONE IN JAW ( 4 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 4 FDA reports)
EYE DISORDER ( 4 FDA reports)
FEAR OF DEATH ( 4 FDA reports)
HAEMORRHAGE ( 4 FDA reports)
HEART RATE DECREASED ( 4 FDA reports)
IMPAIRED WORK ABILITY ( 4 FDA reports)
INJECTION SITE HAEMORRHAGE ( 4 FDA reports)
INJECTION SITE MASS ( 4 FDA reports)
JOINT STIFFNESS ( 4 FDA reports)
LABILE HYPERTENSION ( 4 FDA reports)
LEUKOCYTOSIS ( 4 FDA reports)
LIBIDO DECREASED ( 4 FDA reports)
LOOSE TOOTH ( 4 FDA reports)
MENORRHAGIA ( 4 FDA reports)
MICTURITION URGENCY ( 4 FDA reports)
MIDDLE INSOMNIA ( 4 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 4 FDA reports)
MUSCLE TIGHTNESS ( 4 FDA reports)
PEPTIC ULCER ( 4 FDA reports)
PHOTOSENSITIVITY REACTION ( 4 FDA reports)
PLATELET COUNT DECREASED ( 4 FDA reports)
PSORIATIC ARTHROPATHY ( 4 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 4 FDA reports)
RHINORRHOEA ( 4 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 4 FDA reports)
SEPSIS SYNDROME ( 4 FDA reports)
SEPTIC SHOCK ( 4 FDA reports)
SEROTONIN SYNDROME ( 4 FDA reports)
SINUS TACHYCARDIA ( 4 FDA reports)
SKIN EXFOLIATION ( 4 FDA reports)
SKIN ULCER ( 4 FDA reports)
SLEEP APNOEA SYNDROME ( 4 FDA reports)
STEVENS-JOHNSON SYNDROME ( 4 FDA reports)
STOMATITIS ( 4 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 4 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 4 FDA reports)
TIC ( 4 FDA reports)
UNEVALUABLE EVENT ( 4 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 3 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
AKATHISIA ( 3 FDA reports)
ANAPHYLACTIC REACTION ( 3 FDA reports)
APHAGIA ( 3 FDA reports)
ASPIRATION ( 3 FDA reports)
BLOOD IRON DECREASED ( 3 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 3 FDA reports)
BUNION ( 3 FDA reports)
CARDIO-RESPIRATORY ARREST ( 3 FDA reports)
CEREBRAL THROMBOSIS ( 3 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 3 FDA reports)
CHAPPED LIPS ( 3 FDA reports)
CHOKING ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 3 FDA reports)
CLUMSINESS ( 3 FDA reports)
COLITIS ( 3 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 3 FDA reports)
CRIME ( 3 FDA reports)
DEMENTIA ( 3 FDA reports)
DEPENDENCE ( 3 FDA reports)
DERMAL CYST ( 3 FDA reports)
DISCOMFORT ( 3 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 3 FDA reports)
DRUG TOLERANCE ( 3 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 3 FDA reports)
EPISTAXIS ( 3 FDA reports)
ERYTHEMA MULTIFORME ( 3 FDA reports)
EXOSTOSIS ( 3 FDA reports)
FEELING COLD ( 3 FDA reports)
FEELING JITTERY ( 3 FDA reports)
FOLLICULITIS ( 3 FDA reports)
FUNGAL INFECTION ( 3 FDA reports)
GASTRIC BYPASS ( 3 FDA reports)
GASTRIC ULCER ( 3 FDA reports)
HAND FRACTURE ( 3 FDA reports)
HANGOVER ( 3 FDA reports)
HEARING IMPAIRED ( 3 FDA reports)
HEART RATE IRREGULAR ( 3 FDA reports)
HERPES ZOSTER ( 3 FDA reports)
HIP FRACTURE ( 3 FDA reports)
HUNGER ( 3 FDA reports)
HYPERSOMNIA ( 3 FDA reports)
HYPOPHAGIA ( 3 FDA reports)
HYPORESPONSIVE TO STIMULI ( 3 FDA reports)
IMPAIRED HEALING ( 3 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 3 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 3 FDA reports)
INFLUENZA ( 3 FDA reports)
INJECTION SITE CYST ( 3 FDA reports)
INJECTION SITE DISCHARGE ( 3 FDA reports)
INJECTION SITE DISCOLOURATION ( 3 FDA reports)
INJECTION SITE PRURITUS ( 3 FDA reports)
INJECTION SITE SCAB ( 3 FDA reports)
INJECTION SITE SWELLING ( 3 FDA reports)
INJECTION SITE ULCER ( 3 FDA reports)
INTESTINAL HAEMORRHAGE ( 3 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 3 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 3 FDA reports)
JOINT EFFUSION ( 3 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 3 FDA reports)
LEUKOPENIA ( 3 FDA reports)
LIP DRY ( 3 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 3 FDA reports)
LOCAL SWELLING ( 3 FDA reports)
LOWER LIMB FRACTURE ( 3 FDA reports)
LUNG CONSOLIDATION ( 3 FDA reports)
LYMPHADENOPATHY ( 3 FDA reports)
MUSCLE DISORDER ( 3 FDA reports)
NEPHROLITHIASIS ( 3 FDA reports)
NERVE COMPRESSION ( 3 FDA reports)
OBSESSIVE THOUGHTS ( 3 FDA reports)
ORAL DISCOMFORT ( 3 FDA reports)
OSTEOMYELITIS ( 3 FDA reports)
OVARIAN CANCER ( 3 FDA reports)
PARAESTHESIA ORAL ( 3 FDA reports)
PARALYSIS ( 3 FDA reports)
PELVIC PAIN ( 3 FDA reports)
PETECHIAE ( 3 FDA reports)
PHARYNGITIS ( 3 FDA reports)
PHOTOPHOBIA ( 3 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 3 FDA reports)
PSORIASIS ( 3 FDA reports)
RASH PAPULAR ( 3 FDA reports)
RESPIRATORY DISTRESS ( 3 FDA reports)
SINUS DISORDER ( 3 FDA reports)
SKIN DISCOLOURATION ( 3 FDA reports)
SKIN DISORDER ( 3 FDA reports)
SKIN HYPERPIGMENTATION ( 3 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 3 FDA reports)
SPINAL COLUMN INJURY ( 3 FDA reports)
SPINAL FRACTURE ( 3 FDA reports)
SUICIDAL BEHAVIOUR ( 3 FDA reports)
SUNBURN ( 3 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 3 FDA reports)
TEMPERATURE INTOLERANCE ( 3 FDA reports)
THYROID CANCER ( 3 FDA reports)
THYROID MASS ( 3 FDA reports)
TONGUE ULCERATION ( 3 FDA reports)
UNRESPONSIVE TO STIMULI ( 3 FDA reports)
UTERINE POLYP ( 3 FDA reports)
VAGINAL DISORDER ( 3 FDA reports)
VERY LOW DENSITY LIPOPROTEIN DECREASED ( 3 FDA reports)
VISUAL FIELD DEFECT ( 3 FDA reports)
VITAMIN D DEFICIENCY ( 3 FDA reports)
VITH NERVE PARALYSIS ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
WITHDRAWAL HYPERTENSION ( 3 FDA reports)
WRONG DRUG ADMINISTERED ( 3 FDA reports)
ABDOMINAL HERNIA ( 2 FDA reports)
ABDOMINAL TENDERNESS ( 2 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 2 FDA reports)
ACCIDENTAL EXPOSURE ( 2 FDA reports)
ACUTE SINUSITIS ( 2 FDA reports)
AFFECT LABILITY ( 2 FDA reports)
ANALGESIC THERAPY ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
ANHIDROSIS ( 2 FDA reports)
ANORGASMIA ( 2 FDA reports)
APPARENT DEATH ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
AURA ( 2 FDA reports)
BARTHOLIN'S CYST ( 2 FDA reports)
BASAL CELL CARCINOMA ( 2 FDA reports)
BEDRIDDEN ( 2 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 2 FDA reports)
BLIGHTED OVUM ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD GROWTH HORMONE INCREASED ( 2 FDA reports)
BLOOD TEST ABNORMAL ( 2 FDA reports)
BLOOD URINE PRESENT ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
BREAST CELLULITIS ( 2 FDA reports)
CANDIDIASIS ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CARDIAC MURMUR ( 2 FDA reports)
CARDIOGENIC SHOCK ( 2 FDA reports)
CARDIOVASCULAR DISORDER ( 2 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 2 FDA reports)
CHANGE IN SUSTAINED ATTENTION ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
CONJUNCTIVITIS ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
DEVICE BREAKAGE ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DIABETIC COMA ( 2 FDA reports)
DISABILITY ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DIZZINESS POSTURAL ( 2 FDA reports)
DRUG EFFECT INCREASED ( 2 FDA reports)
DRUG-INDUCED LIVER INJURY ( 2 FDA reports)
DRY EYE ( 2 FDA reports)
DYSGRAPHIA ( 2 FDA reports)
EARLY SATIETY ( 2 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
ERUCTATION ( 2 FDA reports)
ESCHERICHIA INFECTION ( 2 FDA reports)
EXPIRED DRUG ADMINISTERED ( 2 FDA reports)
EYE PAIN ( 2 FDA reports)
EYELID OEDEMA ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
FACIAL SPASM ( 2 FDA reports)
FOOT OPERATION ( 2 FDA reports)
FUNGAL SKIN INFECTION ( 2 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 2 FDA reports)
GALLBLADDER PAIN ( 2 FDA reports)
GASTRIC DISORDER ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
GASTROINTESTINAL PAIN ( 2 FDA reports)
GENITAL DISORDER FEMALE ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HAIR COLOUR CHANGES ( 2 FDA reports)
HALLUCINATIONS, MIXED ( 2 FDA reports)
HEAD TITUBATION ( 2 FDA reports)
HEART INJURY ( 2 FDA reports)
HEAT EXHAUSTION ( 2 FDA reports)
HEPATITIS C ( 2 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 2 FDA reports)
HERNIA ( 2 FDA reports)
HUMERUS FRACTURE ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
ILEUS ( 2 FDA reports)
IMPATIENCE ( 2 FDA reports)
IMPLANT SITE INFECTION ( 2 FDA reports)
INTENTIONAL SELF-INJURY ( 2 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 2 FDA reports)
JOINT INJURY ( 2 FDA reports)
KNEE OPERATION ( 2 FDA reports)
LABORATORY TEST ABNORMAL ( 2 FDA reports)
LARGE INTESTINE PERFORATION ( 2 FDA reports)
LIGAMENT SPRAIN ( 2 FDA reports)
LIMB DISCOMFORT ( 2 FDA reports)
LIP AND/OR ORAL CAVITY CANCER STAGE IV ( 2 FDA reports)
LIPOHYPERTROPHY ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
LYME DISEASE ( 2 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
MACULAR DEGENERATION ( 2 FDA reports)
MATERNAL EXPOSURE BEFORE PREGNANCY ( 2 FDA reports)
MELANOCYTIC NAEVUS ( 2 FDA reports)
MENSTRUATION DELAYED ( 2 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 2 FDA reports)
MOANING ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
MOUTH INJURY ( 2 FDA reports)
MOVEMENT DISORDER ( 2 FDA reports)
MULTIPLE FRACTURES ( 2 FDA reports)
MUSCLE RIGIDITY ( 2 FDA reports)
MYOCLONUS ( 2 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 2 FDA reports)
NEUROPSYCHIATRIC SYNDROME ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
NIPPLE PAIN ( 2 FDA reports)
NIPPLE SWELLING ( 2 FDA reports)
NONSPECIFIC REACTION ( 2 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OEDEMA MOUTH ( 2 FDA reports)
OESOPHAGEAL RUPTURE ( 2 FDA reports)
ORTHOSTATIC HYPOTENSION ( 2 FDA reports)
OVARIAN CYST ( 2 FDA reports)
PAIN IN JAW ( 2 FDA reports)
PAIN OF SKIN ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
PANIC REACTION ( 2 FDA reports)
PAPILLOEDEMA ( 2 FDA reports)
PARATHYROID DISORDER ( 2 FDA reports)
PATIENT-DEVICE INCOMPATIBILITY ( 2 FDA reports)
PERICARDITIS ( 2 FDA reports)
PERIPHERAL COLDNESS ( 2 FDA reports)
PERSONALITY CHANGE ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
POLYCYTHAEMIA ( 2 FDA reports)
POLYDIPSIA ( 2 FDA reports)
POLYMENORRHOEA ( 2 FDA reports)
POST PROCEDURAL INFECTION ( 2 FDA reports)
POST-TRAUMATIC NECK SYNDROME ( 2 FDA reports)
POSTPARTUM DEPRESSION ( 2 FDA reports)
PRE-ECLAMPSIA ( 2 FDA reports)
PRODUCT COUNTERFEIT ( 2 FDA reports)
PRODUCT FORMULATION ISSUE ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PULMONARY INFARCTION ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RASH PUSTULAR ( 2 FDA reports)
REBOUND EFFECT ( 2 FDA reports)
RESPIRATORY RATE INCREASED ( 2 FDA reports)
RETINAL DISORDER ( 2 FDA reports)
RETINAL NEOPLASM ( 2 FDA reports)
SCIATICA ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SELF-MEDICATION ( 2 FDA reports)
SHOCK HAEMORRHAGIC ( 2 FDA reports)
SKELETAL INJURY ( 2 FDA reports)
SKIN BACTERIAL INFECTION ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SKIN WARM ( 2 FDA reports)
SNORING ( 2 FDA reports)
SOCIAL PROBLEM ( 2 FDA reports)
SPINAL CORD INJURY ( 2 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 2 FDA reports)
TENSION ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 2 FDA reports)
THROAT IRRITATION ( 2 FDA reports)
THROMBOSIS IN DEVICE ( 2 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 2 FDA reports)
TONGUE PARALYSIS ( 2 FDA reports)
TONSILLITIS ( 2 FDA reports)
TOOTH LOSS ( 2 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 2 FDA reports)
TRICHIASIS ( 2 FDA reports)
TRISMUS ( 2 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
URINE AMPHETAMINE POSITIVE ( 2 FDA reports)
VAGINAL FISTULA ( 2 FDA reports)
VARICOSE VEIN ( 2 FDA reports)
VASCULAR DEMENTIA ( 2 FDA reports)
VASCULITIS ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
VOMITING PROJECTILE ( 2 FDA reports)
WEIGHT ABNORMAL ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
WRIST FRACTURE ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL ADHESIONS ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABNORMAL FAECES ( 1 FDA reports)
ACARODERMATITIS ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACCIDENTAL DEATH ( 1 FDA reports)
ACNE CYSTIC ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
ALCOHOL ABUSE ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ALLERGIC COLITIS ( 1 FDA reports)
ALLERGY TO ARTHROPOD STING ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
AMBLYOPIA ( 1 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
AMPHETAMINES POSITIVE ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANAL FISTULA ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
ANKYLOSING SPONDYLITIS ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
ANTISOCIAL PERSONALITY DISORDER ( 1 FDA reports)
ANTITHROMBIN III INCREASED ( 1 FDA reports)
ANURIA ( 1 FDA reports)
APATHY ( 1 FDA reports)
APPLICATION SITE RASH ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ARTHROPOD BITE ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
ASTHENOPIA ( 1 FDA reports)
ASTIGMATISM ( 1 FDA reports)
ATRIAL SEPTAL DEFECT ( 1 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 1 FDA reports)
BARRETT'S OESOPHAGUS ( 1 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 1 FDA reports)
BICUSPID AORTIC VALVE ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BILIARY COLIC ( 1 FDA reports)
BINGE DRINKING ( 1 FDA reports)
BIPOLAR I DISORDER ( 1 FDA reports)
BLADDER OPERATION ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD COUNT ABNORMAL ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD INSULIN ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BONE GRAFT ( 1 FDA reports)
BONE LOSS ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BRAIN STEM STROKE ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
BREAST CANCER IN SITU ( 1 FDA reports)
BREAST CYST ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BREAST OEDEMA ( 1 FDA reports)
BREECH PRESENTATION ( 1 FDA reports)
BRONCHITIS ACUTE ( 1 FDA reports)
BRONCHITIS CHRONIC ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
BRUXISM ( 1 FDA reports)
BURSITIS ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CALCULUS URETERIC ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CARDIOSPASM ( 1 FDA reports)
CAROTID ARTERY DISEASE ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CATARACT SUBCAPSULAR ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL CYST ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CEREBRAL PALSY ( 1 FDA reports)
CERUMEN IMPACTION ( 1 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 1 FDA reports)
CERVICITIS ( 1 FDA reports)
CHANGE OF BOWEL HABIT ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHOLANGITIS SCLEROSING ( 1 FDA reports)
CHOREA ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
CLAVICLE FRACTURE ( 1 FDA reports)
CLONUS ( 1 FDA reports)
CLUSTER HEADACHE ( 1 FDA reports)
COITAL BLEEDING ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 1 FDA reports)
COMPLICATED MIGRAINE ( 1 FDA reports)
CORNEAL REFLEX DECREASED ( 1 FDA reports)
CRANIOCEREBRAL INJURY ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CSF VOLUME INCREASED ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DEFORMITY ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEPRESSIVE SYMPTOM ( 1 FDA reports)
DERMATILLOMANIA ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DEVICE ISSUE ( 1 FDA reports)
DEVICE LEAKAGE ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DISSOCIATION ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INTERACTION POTENTIATION ( 1 FDA reports)
DRUG LABEL CONFUSION ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG TOLERANCE INCREASED ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 1 FDA reports)
DYSMENORRHOEA ( 1 FDA reports)
DYSPHORIA ( 1 FDA reports)
DYSPLASIA ( 1 FDA reports)
EAR HAEMORRHAGE ( 1 FDA reports)
EAR INFECTION FUNGAL ( 1 FDA reports)
EATING DISORDER SYMPTOM ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
ECTOPIC PREGNANCY ( 1 FDA reports)
ECTOPIC PREGNANCY WITH INTRAUTERINE DEVICE ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
EDUCATIONAL PROBLEM ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ENURESIS ( 1 FDA reports)
EPICONDYLITIS ( 1 FDA reports)
EROSIVE OESOPHAGITIS ( 1 FDA reports)
ERYTHROMELALGIA ( 1 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYELID FUNCTION DISORDER ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FEMALE SEXUAL DYSFUNCTION ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FOREIGN BODY ( 1 FDA reports)
FRACTURE NONUNION ( 1 FDA reports)
FRONTOTEMPORAL DEMENTIA ( 1 FDA reports)
GALLBLADDER ENLARGEMENT ( 1 FDA reports)
GALLBLADDER OEDEMA ( 1 FDA reports)
GALLBLADDER OPERATION ( 1 FDA reports)
GAMBLING ( 1 FDA reports)
GASTRIC DILATATION ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GENERAL SYMPTOM ( 1 FDA reports)
GENERALISED ANXIETY DISORDER ( 1 FDA reports)
GINGIVAL DISORDER ( 1 FDA reports)
GINGIVITIS ( 1 FDA reports)
GLIOSIS ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
GLYCOSURIA ( 1 FDA reports)
GRAFT COMPLICATION ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
GROWTH RETARDATION ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
HAEMATOCRIT INCREASED ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HALLUCINATION, OLFACTORY ( 1 FDA reports)
HAND-FOOT-AND-MOUTH DISEASE ( 1 FDA reports)
HEAD AND NECK CANCER ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HELICOBACTER TEST POSITIVE ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATITIS B ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HIRSUTISM ( 1 FDA reports)
HOMELESS ( 1 FDA reports)
HOMICIDAL IDEATION ( 1 FDA reports)
HORMONE LEVEL ABNORMAL ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HUMAN BITE ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERACUSIS ( 1 FDA reports)
HYPERMETROPIA ( 1 FDA reports)
HYPERMOBILITY SYNDROME ( 1 FDA reports)
HYPERPARATHYROIDISM ( 1 FDA reports)
HYPERPHAGIA ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
HYPOVITAMINOSIS ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
HYSTERECTOMY ( 1 FDA reports)
ILEAL STENOSIS ( 1 FDA reports)
ILEECTOMY ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
IMPRISONMENT ( 1 FDA reports)
IMPULSE-CONTROL DISORDER ( 1 FDA reports)
INCREASED TENDENCY TO BRUISE ( 1 FDA reports)
INHIBITORY DRUG INTERACTION ( 1 FDA reports)
INJECTION SITE ATROPHY ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
INJECTION SITE PAPULE ( 1 FDA reports)
INJECTION SITE WARMTH ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 1 FDA reports)
INTESTINAL STENOSIS ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JAW OPERATION ( 1 FDA reports)
JOINT ARTHROPLASTY ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
JUDGEMENT IMPAIRED ( 1 FDA reports)
KETOACIDOSIS ( 1 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 1 FDA reports)
KLEPTOMANIA ( 1 FDA reports)
LABILE BLOOD PRESSURE ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LEARNING DISORDER ( 1 FDA reports)
LIMB OPERATION ( 1 FDA reports)
LIMB SALVAGE THERAPY ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LOSS OF LIBIDO ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LOWER EXTREMITY MASS ( 1 FDA reports)
LYMPHOCYTE COUNT NORMAL ( 1 FDA reports)
LYMPHOMATOID PAPULOSIS ( 1 FDA reports)
MAJOR DEPRESSION ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 1 FDA reports)
MEAN CELL VOLUME INCREASED ( 1 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 1 FDA reports)
MENISCUS LESION ( 1 FDA reports)
MENOMETRORRHAGIA ( 1 FDA reports)
MENOPAUSAL SYMPTOMS ( 1 FDA reports)
MENSTRUAL DISORDER ( 1 FDA reports)
MENTAL RETARDATION ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METAPLASIA ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MIGRAINE WITH AURA ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MORTON'S NEUROMA ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MULTIPLE INJURIES ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
NARCOLEPSY ( 1 FDA reports)
NECK INJURY ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
NODULE ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
NYSTAGMUS ( 1 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 1 FDA reports)
OBSESSIVE-COMPULSIVE PERSONALITY DISORDER ( 1 FDA reports)
OCCIPITAL NEURALGIA ( 1 FDA reports)
OESOPHAGEAL STENOSIS ( 1 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
ONYCHOMADESIS ( 1 FDA reports)
OPPOSITIONAL DEFIANT DISORDER ( 1 FDA reports)
OPTIC ATROPHY ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORAL CAVITY FISTULA ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
ORGAN FAILURE ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAINFUL RESPIRATION ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCREATIC CYST ( 1 FDA reports)
PANCREATIC INJURY ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PARENT-CHILD PROBLEM ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PAROTID GLAND ENLARGEMENT ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERIPHERAL EMBOLISM ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PERNICIOUS ANAEMIA ( 1 FDA reports)
PERSECUTORY DELUSION ( 1 FDA reports)
PHOBIA ( 1 FDA reports)
PHOTODERMATOSIS ( 1 FDA reports)
PHYSICAL ABUSE ( 1 FDA reports)
PLANTAR FASCIITIS ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 1 FDA reports)
POISONING ( 1 FDA reports)
POLYCYSTIC OVARIES ( 1 FDA reports)
POLYP ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 1 FDA reports)
PRECANCEROUS SKIN LESION ( 1 FDA reports)
PREGNANCY AFTER POST COITAL CONTRACEPTION ( 1 FDA reports)
PRESBYOPIA ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PRIAPISM ( 1 FDA reports)
PRINZMETAL ANGINA ( 1 FDA reports)
PRODUCT ADHESION ISSUE ( 1 FDA reports)
PRODUCT CONTAMINATION ( 1 FDA reports)
PRODUCT MEASURED POTENCY ISSUE ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROTEIN S INCREASED ( 1 FDA reports)
PROTRUSION TONGUE ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULSE PRESSURE DECREASED ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
RADIAL NERVE PALSY ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RAYNAUD'S PHENOMENON ( 1 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 1 FDA reports)
READING DISORDER ( 1 FDA reports)
RECTAL DISCHARGE ( 1 FDA reports)
RED BLOOD CELL ABNORMALITY ( 1 FDA reports)
REGURGITATION ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RENAL COLIC ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL INFARCT ( 1 FDA reports)
RENAL PAIN ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RHINITIS ALLERGIC ( 1 FDA reports)
RHINITIS SEASONAL ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SCAB ( 1 FDA reports)
SEBORRHOEIC DERMATITIS ( 1 FDA reports)
SECONDARY PROGRESSIVE MULTIPLE SCLEROSIS ( 1 FDA reports)
SELF-INJURIOUS IDEATION ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SEROSITIS ( 1 FDA reports)
SIMPLE PARTIAL SEIZURES ( 1 FDA reports)
SINUS ARRHYTHMIA ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SKIN IRRITATION ( 1 FDA reports)
SKIN MASS ( 1 FDA reports)
SKIN ODOUR ABNORMAL ( 1 FDA reports)
SLUGGISHNESS ( 1 FDA reports)
SOCIAL PHOBIA ( 1 FDA reports)
SOFT TISSUE DISORDER ( 1 FDA reports)
SOLID PSEUDOPAPILLARY TUMOUR OF THE PANCREAS ( 1 FDA reports)
SOMATIC DELUSION ( 1 FDA reports)
SOMNAMBULISM ( 1 FDA reports)
SOTOS' SYNDROME ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
SPLENIC INJURY ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
STRABISMUS ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SWEAT DISCOLOURATION ( 1 FDA reports)
SWEAT GLAND DISORDER ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 1 FDA reports)
TABLET PHYSICAL ISSUE ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TEARFULNESS ( 1 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 1 FDA reports)
TERMINAL INSOMNIA ( 1 FDA reports)
TESTICULAR CYST ( 1 FDA reports)
TESTICULAR PAIN ( 1 FDA reports)
THERAPY CESSATION ( 1 FDA reports)
THERMAL BURN ( 1 FDA reports)
THORACIC OUTLET SYNDROME ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
THYROID NEOPLASM ( 1 FDA reports)
TINEA INFECTION ( 1 FDA reports)
TOBACCO USER ( 1 FDA reports)
TONGUE BITING ( 1 FDA reports)
TONGUE BLISTERING ( 1 FDA reports)
TORTICOLLIS ( 1 FDA reports)
TRAUMATIC LUNG INJURY ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
TRIGGER FINGER ( 1 FDA reports)
TUMOUR RUPTURE ( 1 FDA reports)
TYPE 1 DIABETES MELLITUS ( 1 FDA reports)
ULCER HAEMORRHAGE ( 1 FDA reports)
URETHRAL STENOSIS ( 1 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 1 FDA reports)
UTERINE PAIN ( 1 FDA reports)
VASCULAR RUPTURE ( 1 FDA reports)
VASCULITIS CEREBRAL ( 1 FDA reports)
VERBAL ABUSE ( 1 FDA reports)
VESTIBULITIS ( 1 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VOCAL CORD POLYP ( 1 FDA reports)
VULVOVAGINAL PRURITUS ( 1 FDA reports)
WEIGHT FLUCTUATION ( 1 FDA reports)
WEIGHT GAIN POOR ( 1 FDA reports)
WEIGHT LOSS POOR ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
WOUND ABSCESS ( 1 FDA reports)

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